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Available in 20 languages" > <label id="p-lang-btn-label" for="p-lang-btn-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet cdx-button--action-progressive mw-portlet-lang-heading-20" aria-hidden="true" ><span class="vector-icon mw-ui-icon-language-progressive mw-ui-icon-wikimedia-language-progressive"></span> <span class="vector-dropdown-label-text">20 languages</span> </label> <div class="vector-dropdown-content"> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li class="interlanguage-link interwiki-azb mw-list-item"><a href="https://azb.wikipedia.org/wiki/%D9%86%D9%85%DA%A9_%D8%B2%D8%A7%DB%8C%D8%B3" title="نمک زایس – South Azerbaijani" lang="azb" hreflang="azb" data-title="نمک زایس" data-language-autonym="تۆرکجه" data-language-local-name="South Azerbaijani" class="interlanguage-link-target"><span>تۆرکجه</span></a></li><li class="interlanguage-link interwiki-bn mw-list-item"><a href="https://bn.wikipedia.org/wiki/%E0%A6%9C%E0%A7%87%E0%A6%87%E0%A6%B8%E0%A7%87%E0%A6%B0_%E0%A6%B2%E0%A6%AC%E0%A6%A3" title="জেইসের লবণ – Bangla" lang="bn" hreflang="bn" data-title="জেইসের লবণ" data-language-autonym="বাংলা" data-language-local-name="Bangla" class="interlanguage-link-target"><span>বাংলা</span></a></li><li class="interlanguage-link interwiki-ca mw-list-item"><a href="https://ca.wikipedia.org/wiki/Sal_de_Zeise" title="Sal de Zeise – Catalan" lang="ca" hreflang="ca" data-title="Sal de Zeise" data-language-autonym="Català" data-language-local-name="Catalan" class="interlanguage-link-target"><span>Català</span></a></li><li class="interlanguage-link interwiki-cv mw-list-item"><a href="https://cv.wikipedia.org/wiki/%D0%A6%D0%B5%D0%B9%D0%B7%D0%B5_%D1%82%C4%83%D0%B2%D0%B0%D1%80%C4%95" title="Цейзе тăварĕ – Chuvash" lang="cv" hreflang="cv" data-title="Цейзе тăварĕ" data-language-autonym="Чӑвашла" data-language-local-name="Chuvash" class="interlanguage-link-target"><span>Чӑвашла</span></a></li><li class="interlanguage-link interwiki-cs mw-list-item"><a href="https://cs.wikipedia.org/wiki/Zeiseho_s%C5%AFl" title="Zeiseho sůl – Czech" lang="cs" hreflang="cs" data-title="Zeiseho sůl" data-language-autonym="Čeština" data-language-local-name="Czech" class="interlanguage-link-target"><span>Čeština</span></a></li><li class="interlanguage-link interwiki-de mw-list-item"><a href="https://de.wikipedia.org/wiki/Zeise-Salz" title="Zeise-Salz – German" lang="de" hreflang="de" data-title="Zeise-Salz" data-language-autonym="Deutsch" data-language-local-name="German" class="interlanguage-link-target"><span>Deutsch</span></a></li><li class="interlanguage-link interwiki-es mw-list-item"><a href="https://es.wikipedia.org/wiki/Sal_de_Zeise" title="Sal de Zeise – Spanish" lang="es" hreflang="es" data-title="Sal de Zeise" data-language-autonym="Español" data-language-local-name="Spanish" class="interlanguage-link-target"><span>Español</span></a></li><li class="interlanguage-link interwiki-fa mw-list-item"><a href="https://fa.wikipedia.org/wiki/%D9%86%D9%85%DA%A9_%D8%B2%D8%A7%DB%8C%D8%B3" title="نمک زایس – Persian" lang="fa" hreflang="fa" data-title="نمک زایس" data-language-autonym="فارسی" data-language-local-name="Persian" class="interlanguage-link-target"><span>فارسی</span></a></li><li class="interlanguage-link interwiki-fr mw-list-item"><a href="https://fr.wikipedia.org/wiki/Sel_de_Zeise" title="Sel de Zeise – French" lang="fr" hreflang="fr" data-title="Sel de Zeise" data-language-autonym="Français" data-language-local-name="French" class="interlanguage-link-target"><span>Français</span></a></li><li class="interlanguage-link interwiki-it mw-list-item"><a href="https://it.wikipedia.org/wiki/Sale_di_Zeise" title="Sale di Zeise – Italian" lang="it" hreflang="it" data-title="Sale di Zeise" data-language-autonym="Italiano" data-language-local-name="Italian" class="interlanguage-link-target"><span>Italiano</span></a></li><li class="interlanguage-link interwiki-nl mw-list-item"><a href="https://nl.wikipedia.org/wiki/Kaliumtrichloor(ethyleen)platinaat(II)" title="Kaliumtrichloor(ethyleen)platinaat(II) – Dutch" lang="nl" hreflang="nl" data-title="Kaliumtrichloor(ethyleen)platinaat(II)" data-language-autonym="Nederlands" data-language-local-name="Dutch" class="interlanguage-link-target"><span>Nederlands</span></a></li><li class="interlanguage-link interwiki-ja mw-list-item"><a href="https://ja.wikipedia.org/wiki/%E3%83%84%E3%82%A1%E3%82%A4%E3%82%BC%E5%A1%A9" title="ツァイゼ塩 – Japanese" lang="ja" hreflang="ja" data-title="ツァイゼ塩" data-language-autonym="日本語" data-language-local-name="Japanese" class="interlanguage-link-target"><span>日本語</span></a></li><li class="interlanguage-link interwiki-pt mw-list-item"><a href="https://pt.wikipedia.org/wiki/Sal_de_Zeise" title="Sal de Zeise – Portuguese" lang="pt" hreflang="pt" data-title="Sal de Zeise" data-language-autonym="Português" data-language-local-name="Portuguese" class="interlanguage-link-target"><span>Português</span></a></li><li class="interlanguage-link interwiki-ru mw-list-item"><a href="https://ru.wikipedia.org/wiki/%D0%9C%D0%BE%D0%BD%D0%BE%D0%B3%D0%B8%D0%B4%D1%80%D0%B0%D1%82_%D1%82%D1%80%D0%B8%D1%85%D0%BB%D0%BE%D1%80%D0%BE(%D1%8D%D1%82%D0%B8%D0%BB%D0%B5%D0%BD)%D0%BF%D0%BB%D0%B0%D1%82%D0%B8%D0%BD%D0%B0%D1%82%D0%B0(II)_%D0%BA%D0%B0%D0%BB%D0%B8%D1%8F" title="Моногидрат трихлоро(этилен)платината(II) калия – Russian" lang="ru" hreflang="ru" data-title="Моногидрат трихлоро(этилен)платината(II) калия" data-language-autonym="Русский" data-language-local-name="Russian" class="interlanguage-link-target"><span>Русский</span></a></li><li class="interlanguage-link interwiki-sl mw-list-item"><a href="https://sl.wikipedia.org/wiki/Zeisova_sol" title="Zeisova sol – Slovenian" lang="sl" hreflang="sl" data-title="Zeisova sol" data-language-autonym="Slovenščina" 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mw-list-item"><a href="https://fi.wikipedia.org/wiki/Zeisen_suola" title="Zeisen suola – Finnish" lang="fi" hreflang="fi" data-title="Zeisen suola" data-language-autonym="Suomi" data-language-local-name="Finnish" class="interlanguage-link-target"><span>Suomi</span></a></li><li class="interlanguage-link interwiki-sv mw-list-item"><a href="https://sv.wikipedia.org/wiki/Zeises_salt" title="Zeises salt – Swedish" lang="sv" hreflang="sv" data-title="Zeises salt" data-language-autonym="Svenska" data-language-local-name="Swedish" class="interlanguage-link-target"><span>Svenska</span></a></li><li class="interlanguage-link interwiki-zh mw-list-item"><a href="https://zh.wikipedia.org/wiki/%E8%94%A1%E6%96%AF%E7%9B%90" title="蔡斯盐 – Chinese" lang="zh" hreflang="zh" data-title="蔡斯盐" data-language-autonym="中文" data-language-local-name="Chinese" class="interlanguage-link-target"><span>中文</span></a></li> </ul> <div class="after-portlet after-portlet-lang"><span class="wb-langlinks-edit 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<div id="contentSub"><div id="mw-content-subtitle"><div class="cdx-message cdx-message--block cdx-message--warning mw-revision"><span class="cdx-message__icon"></span><div class="cdx-message__content"><div id="mw-revision-info"><p><b>This is an <a href="/wiki/Help:Page_history" title="Help:Page history">old revision</a> of this page, as edited by <span id="mw-revision-name"><a href="/wiki/User:Headbomb" class="mw-userlink" title="User:Headbomb" data-mw-revid="1260140558"><bdi>Headbomb</bdi></a> <span class="mw-usertoollinks">(<a href="/wiki/User_talk:Headbomb" class="mw-usertoollinks-talk" title="User talk:Headbomb">talk</a> | <a href="/wiki/Special:Contributions/Headbomb" class="mw-usertoollinks-contribs" title="Special:Contributions/Headbomb">contribs</a>)</span></span> at <span id="mw-revision-date">02:54, 29 November 2024</span><span id="mw-revision-summary"> <span class="comment">(<span class="autocomment"><a href="#Preparation">→<bdi dir="ltr">Preparation</bdi></a>: </span> clean 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The present address (URL) is a <a href="/wiki/Help:Permanent_link" title="Help:Permanent link">permanent link</a> to this revision, which may differ significantly from the <span class="plainlinks"><a class="external text" href="https://en.wikipedia.org/wiki/Zeise%27s_salt">current revision</a></span>.</b></p><div id="revision-info-plain" style="display: none;">Revision as of 02:54, 29 November 2024 by <a href="/wiki/User:Headbomb" class="mw-userlink" title="User:Headbomb" data-mw-revid="1260140558"><bdi>Headbomb</bdi></a> <span class="mw-usertoollinks">(<a href="/wiki/User_talk:Headbomb" class="mw-usertoollinks-talk" title="User talk:Headbomb">talk</a> | <a href="/wiki/Special:Contributions/Headbomb" class="mw-usertoollinks-contribs" title="Special:Contributions/Headbomb">contribs</a>)</span> <span class="comment">(<span class="autocomment"><a href="#Preparation">→<bdi dir="ltr">Preparation</bdi></a>: </span> clean up)</span></div></div><div id="mw-revision-nav">(<a href="/w/index.php?title=Zeise%27s_salt&diff=prev&oldid=1260140558" title="Zeise's salt">diff</a>) <a href="/w/index.php?title=Zeise%27s_salt&direction=prev&oldid=1260140558" title="Zeise's salt">← Previous revision</a> | <a href="/wiki/Zeise%27s_salt" title="Zeise's salt">Latest revision</a> (<a href="/w/index.php?title=Zeise%27s_salt&diff=cur&oldid=1260140558" title="Zeise's salt">diff</a>) | <a href="/w/index.php?title=Zeise%27s_salt&direction=next&oldid=1260140558" title="Zeise's salt">Newer revision →</a> (<a href="/w/index.php?title=Zeise%27s_salt&diff=next&oldid=1260140558" title="Zeise's salt">diff</a>)</div></div></div></div></div> <div id="mw-content-text" class="mw-body-content"><div class="mw-content-ltr mw-parser-output" lang="en" dir="ltr"><style data-mw-deduplicate="TemplateStyles:r1084375498">.mw-parser-output .ib-chembox{border-collapse:collapse;text-align:left}.mw-parser-output .ib-chembox td,.mw-parser-output .ib-chembox th{border:1px solid #a2a9b1;width:40%}.mw-parser-output .ib-chembox td+td{width:60%}</style> <table class="infobox ib-chembox"> <caption>Zeise's salt<sup id="cite_ref-1" class="reference"><a href="#cite_note-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup> </caption> <tbody><tr> <td colspan="2" style="text-align:center; padding:2px;"><span typeof="mw:File"><a href="/wiki/File:Zeise%27s-salt-anion-from-xtal-3D-balls.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c7/Zeise%27s-salt-anion-from-xtal-3D-balls.png/220px-Zeise%27s-salt-anion-from-xtal-3D-balls.png" decoding="async" width="220" height="146" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c7/Zeise%27s-salt-anion-from-xtal-3D-balls.png/330px-Zeise%27s-salt-anion-from-xtal-3D-balls.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c7/Zeise%27s-salt-anion-from-xtal-3D-balls.png/440px-Zeise%27s-salt-anion-from-xtal-3D-balls.png 2x" data-file-width="1100" data-file-height="731" /></a></span> </td></tr> <tr> <td colspan="2" style="text-align:center; padding:2px;"><span typeof="mw:File"><a href="/wiki/File:Zeise%27sSalt.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/41/Zeise%27sSalt.png/220px-Zeise%27sSalt.png" decoding="async" width="220" height="153" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/41/Zeise%27sSalt.png/330px-Zeise%27sSalt.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/41/Zeise%27sSalt.png/440px-Zeise%27sSalt.png 2x" data-file-width="471" data-file-height="328" /></a></span> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Names </th></tr> <tr> <td colspan="2" style="text-align:left;"><a href="/wiki/Chemical_nomenclature" title="Chemical nomenclature">IUPAC name</a> <div style="max-width:22em; word-wrap:break-word; padding-left:1.7em;">Potassium trichloro(ethylene)platinate(II) hydrate</div> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Identifiers </th></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/CAS_Registry_Number" title="CAS Registry Number">CAS Number</a></div> </td> <td><style data-mw-deduplicate="TemplateStyles:r1126788409">.mw-parser-output .plainlist ol,.mw-parser-output .plainlist ul{line-height:inherit;list-style:none;margin:0;padding:0}.mw-parser-output .plainlist ol li,.mw-parser-output .plainlist ul li{margin-bottom:0}</style><div class="plainlist"><ul><li><span title="commonchemistry.cas.org"><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=16405-35-9">16405-35-9</a></span><sup> <span typeof="mw:File"><span><img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" /></span></span><span style="display:none">Y</span></sup></li></ul></div> </td></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;">3D model (<a href="/wiki/JSmol" class="mw-redirect" title="JSmol">JSmol</a>)</div> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><span title="chemapps.stolaf.edu (3D interactive model)"><a rel="nofollow" class="external text" href="https://chemapps.stolaf.edu/jmol/jmol.php?model=%5BK%2B%5D.C%3DC.Cl%5BPt-%5D%28Cl%29Cl.O">Interactive image</a></span></li></ul></div> </td></tr> <tr> <td><a href="/wiki/ChemSpider" title="ChemSpider">ChemSpider</a> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><span title="www.chemspider.com"><a rel="nofollow" class="external text" href="https://www.chemspider.com/Chemical-Structure.21241825.html">21241825</a></span></li></ul></div> </td></tr> <tr> <td><a href="/wiki/ECHA_InfoCard" class="mw-redirect" title="ECHA InfoCard"><span title="echa.europa.eu">ECHA InfoCard</span></a> </td> <td><a rel="nofollow" class="external text" href="https://echa.europa.eu/substance-information/-/substanceinfo/100.158.770">100.158.770</a> <span class="mw-valign-text-top noprint" typeof="mw:File/Frameless"><a href="https://www.wikidata.org/wiki/Q184967#P2566" title="Edit this at Wikidata"><img alt="Edit this at Wikidata" src="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png" decoding="async" width="10" height="10" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/15px-OOjs_UI_icon_edit-ltr-progressive.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/20px-OOjs_UI_icon_edit-ltr-progressive.svg.png 2x" data-file-width="20" data-file-height="20" /></a></span> </td></tr> <tr> <td><a href="/wiki/European_Community_number" title="European Community number"><span title="European Community number (chemical identifier)">EC Number</span></a> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li>630-445-1</li></ul></div> </td></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/PubChem" title="PubChem">PubChem</a> <abbr title="Compound ID">CID</abbr></div> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><span title="pubchem.ncbi.nlm.nih.gov"><a rel="nofollow" class="external text" href="https://pubchem.ncbi.nlm.nih.gov/compound/193510">193510</a></span></li></ul></div> </td></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/CompTox_Chemicals_Dashboard" title="CompTox Chemicals Dashboard">CompTox Dashboard</a> <span style="font-weight:normal">(<abbr title="U.S. Environmental Protection Agency">EPA</abbr>)</span></div> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><span title="comptox.epa.gov"><a rel="nofollow" class="external text" href="https://comptox.epa.gov/dashboard/chemical/details/DTXSID90936900">DTXSID90936900</a> <span class="mw-valign-text-top noprint" typeof="mw:File/Frameless"><a href="https://www.wikidata.org/wiki/Q184967#P3117" title="Edit this at Wikidata"><img alt="Edit this at Wikidata" src="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png" decoding="async" width="10" height="10" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/15px-OOjs_UI_icon_edit-ltr-progressive.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/20px-OOjs_UI_icon_edit-ltr-progressive.svg.png 2x" data-file-width="20" data-file-height="20" /></a></span></span></li></ul></div> </td></tr> <tr> <td colspan="2"><div class="collapsible-list mw-collapsible mw-collapsed" style="text-align: left;"> <div style="line-height: 1.6em; font-weight: bold; text-align:left; font-weight:normal; background:transparent;"><div><a href="/wiki/International_Chemical_Identifier" title="International Chemical Identifier">InChI</a></div></div> <ul class="mw-collapsible-content" style="margin-top: 0; margin-bottom: 0; line-height: inherit; list-style: none; margin-left: 0; word-break:break-all;"><li style="line-height: inherit; margin: 0"><div style="border-top:1px solid #ccc; padding:0.2em 0 0.2em 1.5em; text-align:left;"><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">InChI=1S/C2H4.3ClH.K.H2O.Pt/c1-2;;;;;;/h1-2H2;3*1H;;1H2;/q;;;;+1;;+2/p-3</div><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">Key: DCEGWIMEFFONKJ-UHFFFAOYSA-K</div></div></li></ul> </div> </td></tr> <tr> <td colspan="2"><div class="collapsible-list mw-collapsible mw-collapsed" style="text-align: left;"> <div style="line-height: 1.6em; font-weight: bold; text-align:left; font-weight:normal; background:transparent;"><div><a href="/wiki/Simplified_molecular-input_line-entry_system" class="mw-redirect" title="Simplified molecular-input line-entry system">SMILES</a></div></div> <ul class="mw-collapsible-content" style="margin-top: 0; margin-bottom: 0; line-height: inherit; list-style: none; margin-left: 0; word-break:break-all;"><li style="line-height: inherit; margin: 0"><div style="border-top:1px solid #ccc; padding:0.2em 0 0.2em 1.6em; word-wrap:break-word; text-indent:-1.5em; text-align:left; font-size:97%; line-height:120%;">[K+].C=C.Cl[Pt-](Cl)Cl.O</div></li></ul> </div> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Properties </th></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/Chemical_formula" title="Chemical formula">Chemical formula</a></div> </td> <td><span title="Carbon">C</span><sub>2</sub><span title="Hydrogen">H</span><sub>6</sub><span title="Chlorine">Cl</span><sub>3</sub><span title="Potassium">K</span><span title="Oxygen">O</span><span title="Platinum">Pt</span> </td></tr> <tr> <td><a href="/wiki/Molar_mass" title="Molar mass">Molar mass</a> </td> <td><span class="nowrap"><span data-sort-value="7002386600000000000♠"></span>386.60</span> g·mol<sup>−1</sup>   </td></tr> <tr> <td>Appearance </td> <td>Yellow to orange crystals </td></tr> <tr> <td><a href="/wiki/Melting_point" title="Melting point">Melting point</a> </td> <td>220 °C </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Hazards </th></tr> <tr> <td colspan="2" style="text-align:left; background-color:#eaeaea;"><a href="/wiki/Globally_Harmonized_System_of_Classification_and_Labelling_of_Chemicals" title="Globally Harmonized System of Classification and Labelling of Chemicals"><b>GHS</b> labelling</a>:<sup id="cite_ref-2" class="reference"><a href="#cite_note-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> </td></tr> <tr> <td style="padding-left:1em;"><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/GHS_hazard_pictograms" title="GHS hazard pictograms">Pictograms</a></div> </td> <td><span typeof="mw:File"><a href="/wiki/File:GHS-pictogram-exclam.svg" class="mw-file-description" title="GHS07: Exclamation mark"><img alt="GHS07: Exclamation mark" src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c3/GHS-pictogram-exclam.svg/50px-GHS-pictogram-exclam.svg.png" decoding="async" width="50" height="50" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c3/GHS-pictogram-exclam.svg/75px-GHS-pictogram-exclam.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c3/GHS-pictogram-exclam.svg/100px-GHS-pictogram-exclam.svg.png 2x" data-file-width="512" data-file-height="512" /></a></span> </td></tr> <tr> <td style="padding-left:1em;"><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/Globally_Harmonized_System_of_Classification_and_Labelling_of_Chemicals#Signal_word" title="Globally Harmonized System of Classification and Labelling of Chemicals">Signal word</a></div> </td> <td><b>Warning</b> </td></tr> <tr> <td style="padding-left:1em;"><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/GHS_hazard_statements" title="GHS hazard statements">Hazard statements</a></div> </td> <td><abbr class="abbr" title="H315: Causes skin irritation">H315</abbr>, <abbr class="abbr" title="H319: Causes serious eye irritation">H319</abbr>, <abbr class="abbr" title="H335: May cause respiratory irritation">H335</abbr> </td></tr> <tr> <td colspan="2" style="text-align:left; background:#f8eaba; border:1px solid #a2a9b1;"><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;">Except where otherwise noted, data are given for materials in their <a href="/wiki/Standard_state" title="Standard state">standard state</a> (at 25 °C [77 °F], 100 kPa).</div> <div style="margin-top: 0.3em;"><div style="text-align:center;"><span typeof="mw:File"><span><img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/12px-Yes_check.svg.png" decoding="async" width="12" height="12" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/18px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/24px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" /></span></span><span style="display:none">Y</span> <span class="reflink plainlinks nourlexpansion"><a class="external text" href="https://en.wikipedia.org/w/index.php?title=Special:ComparePages&rev1=437377355&page2=Zeise%26%2339%3Bs+salt">verify</a></span> (<a href="/wiki/Wikipedia:WikiProject_Chemicals/Chembox_validation" title="Wikipedia:WikiProject Chemicals/Chembox validation">what is</a> <sup><span typeof="mw:File"><span><img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" /></span></span><span style="display:none">Y</span><span typeof="mw:File"><span><img alt="☒" src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/7px-X_mark.svg.png" decoding="async" width="7" height="8" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/11px-X_mark.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/14px-X_mark.svg.png 2x" data-file-width="525" data-file-height="600" /></span></span><span style="display:none">N</span></sup> ?) </div></div> <div style="margin-top: 0.3em; text-align: center;"><a href="/wiki/Wikipedia:Chemical_infobox#References" title="Wikipedia:Chemical infobox">Infobox references</a></div> </td></tr> </tbody></table><div class="shortdescription nomobile noexcerpt noprint searchaux" style="display:none">Chemical compound</div> <p><b>Zeise's salt</b>, potassium trichloro(ethylene)platinate(II) hydrate, is the <a href="/wiki/Chemical_compound" title="Chemical compound">chemical compound</a> with the <a href="/wiki/Chemical_formula" title="Chemical formula">formula</a> K[<a href="/wiki/Platinum" title="Platinum">Pt</a>Cl<sub>3</sub>(C<sub>2</sub>H<sub>4</sub>)]·H<sub>2</sub>O. The anion of this air-stable, yellow, <a href="/wiki/Complex_(chemistry)" class="mw-redirect" title="Complex (chemistry)">coordination complex</a> contains an <a href="/wiki/Hapticity" title="Hapticity"><i>η</i><sup>2</sup></a>-<a href="/wiki/Ethylene" title="Ethylene">ethylene</a> <a href="/wiki/Ligand" title="Ligand">ligand</a>. The anion features a platinum atom with a <a href="/wiki/Square_planar" class="mw-redirect" title="Square planar">square planar</a> geometry. The salt is of historical importance in the area of <a href="/wiki/Organometallic_chemistry" title="Organometallic chemistry">organometallic chemistry</a> as one of the first examples of a <a href="/wiki/Transition_metal_alkene_complex" title="Transition metal alkene complex">transition metal alkene complex</a> and is named for its discoverer, <a href="/wiki/William_Christopher_Zeise" title="William Christopher Zeise">William Christopher Zeise</a>. </p> <meta property="mw:PageProp/toc" /> <div class="mw-heading mw-heading2"><h2 id="Preparation">Preparation</h2></div> <p>This compound is commercially available as a hydrate. The hydrate is commonly prepared from <a href="/wiki/Potassium_tetrachloroplatinate" title="Potassium tetrachloroplatinate">K<sub>2</sub>[PtCl<sub>4</sub>]</a> and <a href="/wiki/Ethylene" title="Ethylene">ethylene</a> in the presence of a <a href="/wiki/Catalyst" class="mw-redirect" title="Catalyst">catalytic</a> amount of <a href="/wiki/Tin(II)_chloride" title="Tin(II) chloride">SnCl<sub>2</sub></a>. The water of hydration can be removed <i>in vacuo</i>.<sup id="cite_ref-3" class="reference"><a href="#cite_note-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup> </p> <div class="mw-heading mw-heading2"><h2 id="Structure">Structure</h2></div> <p>The alkene C=C bond is approximately perpendicular to the PtCl<sub>3</sub> plane.<sup id="cite_ref-4" class="reference"><a href="#cite_note-4"><span class="cite-bracket">[</span>4<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-5" class="reference"><a href="#cite_note-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup> In Zeise's salt and related compounds, the alkene rotates about the metal-alkene bond with a modest <a href="/wiki/Activation_energy" title="Activation energy">activation energy</a>. Analysis of the barrier heights indicates that the π-bonding between most metals and the alkene is weaker than the σ-bonding. In Zeise's anion, this rotational barrier has not been assessed. </p> <div class="mw-heading mw-heading2"><h2 id="History">History</h2></div> <p>Zeise's salt was one of the first <a href="/wiki/Organometallic_chemistry" title="Organometallic chemistry">organometallic</a> compounds to be reported.<sup id="cite_ref-6" class="reference"><a href="#cite_note-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup> It was discovered by <a href="/wiki/William_Christopher_Zeise" title="William Christopher Zeise">William Christopher Zeise</a>, a professor at the <a href="/wiki/University_of_Copenhagen" title="University of Copenhagen">University of Copenhagen</a>, who prepared this compound in 1830 while investigating the reaction of <a href="/wiki/Platinum(IV)_chloride" title="Platinum(IV) chloride">PtCl<sub>4</sub></a> with boiling <a href="/wiki/Ethanol" title="Ethanol">ethanol</a>. Following careful analysis he proposed that the resulting compound contained <a href="/wiki/Ethylene" title="Ethylene">ethylene</a>. <a href="/wiki/Justus_von_Liebig" title="Justus von Liebig">Justus von Liebig</a>, a highly influential chemist of that era, often criticised Zeise's proposal, but Zeise's proposal was decisively supported in 1868 when Birnbaum prepared the complex using ethylene.<sup id="cite_ref-7" class="reference"><a href="#cite_note-7"><span class="cite-bracket">[</span>7<span class="cite-bracket">]</span></a></sup> Zeise's salt received a great deal of attention during the second half of the 19th century because chemists could not explain its <a href="/wiki/Molecular_structure" class="mw-redirect" title="Molecular structure">molecular structure</a>. This question remained unanswered until the determination of its <a href="/wiki/X-ray_crystallography" title="X-ray crystallography">X-ray crystal structure</a> in the 20th century.<sup id="cite_ref-8" class="reference"><a href="#cite_note-8"><span class="cite-bracket">[</span>8<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-9" class="reference"><a href="#cite_note-9"><span class="cite-bracket">[</span>9<span class="cite-bracket">]</span></a></sup> Zeise's salt stimulated much scientific research in the field of <a href="/wiki/Organometallic_chemistry" title="Organometallic chemistry">organometallic chemistry</a> and would be key in defining new concepts in chemistry. The <a href="/wiki/Dewar%E2%80%93Chatt%E2%80%93Duncanson_model" title="Dewar–Chatt–Duncanson model">Dewar–Chatt–Duncanson model</a> explains how the metal is coordinated to the C=C double bond.<sup id="cite_ref-10" class="reference"><a href="#cite_note-10"><span class="cite-bracket">[</span>10<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-11" class="reference"><a href="#cite_note-11"><span class="cite-bracket">[</span>11<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-12" class="reference"><a href="#cite_note-12"><span class="cite-bracket">[</span>12<span class="cite-bracket">]</span></a></sup> </p> <div class="mw-heading mw-heading2"><h2 id="Related_compounds">Related compounds</h2></div> <ul><li>Zeise's dimer, [(<i>η</i><sup>2</sup>-C<sub>2</sub>H<sub>4</sub>)PtCl<sub>2</sub>]<sub>2</sub>, derived from Zeise's salt by elimination of KCl followed by dimerisation.</li> <li>COD-platinum dichloride, <a href="/wiki/Dichloro(cycloocta-1,5-diene)platinum(II)" title="Dichloro(cycloocta-1,5-diene)platinum(II)">(cyclooctadiene)PtCl<sub>2</sub></a>, derived from <a href="/wiki/Platinum(II)_chloride" title="Platinum(II) chloride">platinum(II) chloride</a> and <a href="/wiki/1,5-cyclooctadiene" class="mw-redirect" title="1,5-cyclooctadiene">1,5-cyclooctadiene</a>, is a common platinum(II) alkene complex.</li></ul> <p>Many other ethylene complexes have been prepared. For example, ethylenebis(triphenylphosphine)platinum(0), [(C<sub>6</sub>H<sub>5</sub>)<sub>3</sub>P]<sub>2</sub>Pt(H<sub>2</sub>C=CH<sub>2</sub>), wherein the platinum is three-coordinate and in <a href="/wiki/Oxidation_state" title="Oxidation state">oxidation state</a> 0 (Zeise's salt is a derivative of platinum(II)). </p> <ul><li>Dichloro(ethylene)(α-<a href="/wiki/Methylbenzylamine" class="mw-redirect" title="Methylbenzylamine">methylbenzylamine</a>)platinum(II) (PtCl<sub>2</sub>(C<sub>2</sub>H<sub>4</sub>)(PhCH(NH<sub>2</sub>)Me) is a chiral derivative of Zeise's salt that is used for the <a href="/wiki/Chiral_resolution" title="Chiral resolution">chiral resolution</a> of alkenes.<sup id="cite_ref-13" class="reference"><a href="#cite_note-13"><span class="cite-bracket">[</span>13<span class="cite-bracket">]</span></a></sup></li></ul> <div class="mw-heading mw-heading2"><h2 id="References">References</h2></div> <style data-mw-deduplicate="TemplateStyles:r1239543626">.mw-parser-output .reflist{margin-bottom:0.5em;list-style-type:decimal}@media screen{.mw-parser-output .reflist{font-size:90%}}.mw-parser-output .reflist .references{font-size:100%;margin-bottom:0;list-style-type:inherit}.mw-parser-output .reflist-columns-2{column-width:30em}.mw-parser-output .reflist-columns-3{column-width:25em}.mw-parser-output .reflist-columns{margin-top:0.3em}.mw-parser-output .reflist-columns ol{margin-top:0}.mw-parser-output .reflist-columns li{page-break-inside:avoid;break-inside:avoid-column}.mw-parser-output .reflist-upper-alpha{list-style-type:upper-alpha}.mw-parser-output .reflist-upper-roman{list-style-type:upper-roman}.mw-parser-output .reflist-lower-alpha{list-style-type:lower-alpha}.mw-parser-output .reflist-lower-greek{list-style-type:lower-greek}.mw-parser-output .reflist-lower-roman{list-style-type:lower-roman}</style><div class="reflist"> <div class="mw-references-wrap mw-references-columns"><ol 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a{background:url("//upload.wikimedia.org/wikipedia/commons/d/d6/Lock-gray-alt-2.svg")right 0.1em center/9px no-repeat}.mw-parser-output .id-lock-subscription.id-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/a/aa/Lock-red-alt-2.svg")right 0.1em center/9px no-repeat}.mw-parser-output .cs1-ws-icon a{background:url("//upload.wikimedia.org/wikipedia/commons/4/4c/Wikisource-logo.svg")right 0.1em center/12px no-repeat}body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-free a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-limited a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-registration a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-subscription a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .cs1-ws-icon a{background-size:contain;padding:0 1em 0 0}.mw-parser-output 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B.; Halpern, J.; Paulik, F. E.; Shupack, Saul I.; Deangelis, Thomas P. (January 1990). "Potassium Trichloro(Ethene)Platinate(II) (Zeise's Salt)". <i><a href="/wiki/Inorganic_Syntheses" title="Inorganic Syntheses">Inorg. 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"The crystal and molecular structure of Zeise's salt, KPtCl<sub>3</sub>·C<sub>2</sub>H<sub>4</sub>·H<sub>2</sub>O". <i><a href="/wiki/Acta_Crystallographica" title="Acta Crystallographica">Acta Crystallogr.</a></i> <b>B25</b> (9): 1753–1759. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1107%2FS0567740869004699">10.1107/S0567740869004699</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Acta+Crystallogr.&rft.atitle=The+crystal+and+molecular+structure+of+Zeise%27s+salt%2C+KPtCl%3Csub%3E3%3C%2Fsub%3E%C2%B7C%3Csub%3E2%3C%2Fsub%3EH%3Csub%3E4%3C%2Fsub%3E%C2%B7H%3Csub%3E2%3C%2Fsub%3EO&rft.volume=B25&rft.issue=9&rft.pages=1753-1759&rft.date=1969&rft_id=info%3Adoi%2F10.1107%2FS0567740869004699&rft.aulast=Black&rft.aufirst=M.&rft.au=Mais%2C+R.+H.+B.&rft.au=Owston%2C+P.+G.&rfr_id=info%3Asid%2Fen.wikipedia.org%3AZeise%27s+salt" class="Z3988"></span></span> </li> <li id="cite_note-5"><span class="mw-cite-backlink"><b><a href="#cite_ref-5">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFLoveKoetzleWilliamsAndrews1975" class="citation journal cs1">Love, R. A.; Koetzle, T. F.; Williams, G. J. B.; Andrews, L. C.; Bau, R. (1975). "Neutron diffraction study of the structure of Zeise's salt, KPtCl<sub>3</sub>·C<sub>2</sub>H<sub>4</sub>·H<sub>2</sub>O". <i><a href="/wiki/Inorganic_Chemistry_(journal)" title="Inorganic Chemistry (journal)">Inorg. 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Chem.</a></i> (in German). <b>97</b> (4): 497–541. <a href="/wiki/Bibcode_(identifier)" class="mw-redirect" title="Bibcode (identifier)">Bibcode</a>:<a rel="nofollow" class="external text" href="https://ui.adsabs.harvard.edu/abs/1831AnP....97..497Z">1831AnP....97..497Z</a>. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1002%2Fandp.18310970402">10.1002/andp.18310970402</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Ann.+Phys.+Chem.&rft.atitle=Von+der+Wirkung+zwischen+Platinchlorid+und+Alkohol%2C+und+von+den+dabei+entstehenden+neuen+Substanzen&rft.volume=97&rft.issue=4&rft.pages=497-541&rft.date=1831&rft_id=info%3Adoi%2F10.1002%2Fandp.18310970402&rft_id=info%3Abibcode%2F1831AnP....97..497Z&rft.aulast=Zeise&rft.aufirst=W.+C.&rft_id=https%3A%2F%2Fzenodo.org%2Frecord%2F1423546&rfr_id=info%3Asid%2Fen.wikipedia.org%3AZeise%27s+salt" class="Z3988"></span></span> </li> <li id="cite_note-7"><span class="mw-cite-backlink"><b><a href="#cite_ref-7">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFHunt1984" class="citation journal cs1">Hunt, L. 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Archived from <a rel="nofollow" class="external text" href="https://technology.matthey.com/documents/496120/626258/pmr-v28-i2-076-083.pdf/bcda1a2a-3ef1-cbda-19a7-062e2dabd43e?version=1.0&t=1656013811978">the original</a> on 2023-05-22<span class="reference-accessdate">. Retrieved <span class="nowrap">2022-09-28</span></span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Platin.+Met.+Rev.&rft.atitle=The+First+Organometallic+Compounds%3A+William+Christopher+Zeise+and+His+Platinum+Complexes&rft.volume=28&rft.issue=2&rft.pages=76-83&rft.date=1984&rft_id=info%3Adoi%2F10.1595%2F003214084X2827683&rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A100304495%23id-name%3DS2CID&rft.aulast=Hunt&rft.aufirst=L.+B.&rft_id=https%3A%2F%2Ftechnology.matthey.com%2Fdocuments%2F496120%2F626258%2Fpmr-v28-i2-076-083.pdf%2Fbcda1a2a-3ef1-cbda-19a7-062e2dabd43e%3Fversion%3D1.0%26t%3D1656013811978&rfr_id=info%3Asid%2Fen.wikipedia.org%3AZeise%27s+salt" class="Z3988"></span></span> </li> <li id="cite_note-8"><span class="mw-cite-backlink"><b><a href="#cite_ref-8">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFBlackMaisOwston1969" class="citation journal cs1">Black, M.; Mais, R. 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B</a></i>. <b>25</b> (9): 1753–1759. <a href="/wiki/Bibcode_(identifier)" class="mw-redirect" title="Bibcode (identifier)">Bibcode</a>:<a rel="nofollow" class="external text" href="https://ui.adsabs.harvard.edu/abs/1969AcCrB..25.1753B">1969AcCrB..25.1753B</a>. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1107%2FS0567740869004699">10.1107/S0567740869004699</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Acta+Crystallogr.+B&rft.atitle=The+crystal+and+molecular+structure+of+Zeise%27s+salt%2C+KPtCl%3Csub%3E3%3C%2Fsub%3E.C%3Csub%3E2%3C%2Fsub%3EH%3Csub%3E4%3C%2Fsub%3E.H%3Csub%3E2%3C%2Fsub%3EO&rft.volume=25&rft.issue=9&rft.pages=1753-1759&rft.date=1969&rft_id=info%3Adoi%2F10.1107%2FS0567740869004699&rft_id=info%3Abibcode%2F1969AcCrB..25.1753B&rft.aulast=Black&rft.aufirst=M.&rft.au=Mais%2C+R.+H.+B.&rft.au=Owston%2C+P.+G.&rfr_id=info%3Asid%2Fen.wikipedia.org%3AZeise%27s+salt" class="Z3988"></span></span> </li> <li id="cite_note-9"><span class="mw-cite-backlink"><b><a href="#cite_ref-9">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFJarvisKilbournOwston1971" class="citation journal cs1">Jarvis, J. 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B</a></i>. <b>27</b> (2): 366–372. <a href="/wiki/Bibcode_(identifier)" class="mw-redirect" title="Bibcode (identifier)">Bibcode</a>:<a rel="nofollow" class="external text" href="https://ui.adsabs.harvard.edu/abs/1971AcCrB..27..366J">1971AcCrB..27..366J</a>. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1107%2FS0567740871002231">10.1107/S0567740871002231</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Acta+Crystallogr.+B&rft.atitle=A+Re-determination+of+the+Crystal+and+Molecular+Structure+of+Zeise%27s+salt%2C+KPtCl%3Csub%3E3%3C%2Fsub%3E.C%3Csub%3E2%3C%2Fsub%3EH%3Csub%3E4%3C%2Fsub%3E.H%3Csub%3E2%3C%2Fsub%3EO&rft.volume=27&rft.issue=2&rft.pages=366-372&rft.date=1971&rft_id=info%3Adoi%2F10.1107%2FS0567740871002231&rft_id=info%3Abibcode%2F1971AcCrB..27..366J&rft.aulast=Jarvis&rft.aufirst=J.+A.+J.&rft.au=Kilbourn%2C+B.+T.&rft.au=Owston%2C+P.+G.&rfr_id=info%3Asid%2Fen.wikipedia.org%3AZeise%27s+salt" class="Z3988"></span></span> </li> <li id="cite_note-10"><span class="mw-cite-backlink"><b><a href="#cite_ref-10">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFMingos2001" class="citation journal cs1"><a href="/wiki/Michael_Mingos" title="Michael Mingos">Mingos, D. Michael P.</a> (2001). "A Historical Perspective on Dewar's Landmark Contribution to Organometallic Chemistry". <i><a href="/wiki/J._Organomet._Chem." class="mw-redirect" title="J. Organomet. Chem.">J. Organomet. Chem.</a></i> <b>635</b> (1–2): 1–8. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2FS0022-328X%2801%2901155-X">10.1016/S0022-328X(01)01155-X</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=J.+Organomet.+Chem.&rft.atitle=A+Historical+Perspective+on+Dewar%27s+Landmark+Contribution+to+Organometallic+Chemistry&rft.volume=635&rft.issue=1%E2%80%932&rft.pages=1-8&rft.date=2001&rft_id=info%3Adoi%2F10.1016%2FS0022-328X%2801%2901155-X&rft.aulast=Mingos&rft.aufirst=D.+Michael+P.&rfr_id=info%3Asid%2Fen.wikipedia.org%3AZeise%27s+salt" class="Z3988"></span></span> </li> <li id="cite_note-11"><span class="mw-cite-backlink"><b><a href="#cite_ref-11">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFWinterton2002" class="citation book cs1">Winterton, N. (2002). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=VoBxtPb5zCcC&pg=PA103">"Some Notes on the Early Development of Models of Bonding in Olefin-Metal Complexes"</a>. In Leigh, G. J.; Winterton, N. (eds.). <i>Modern Coordination Chemistry: The Legacy of Joseph Chatt</i>. <a href="/wiki/RSC_Publishing" class="mw-redirect" title="RSC Publishing">RSC Publishing</a>. pp. 103–110. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-0-85404-469-6" title="Special:BookSources/978-0-85404-469-6"><bdi>978-0-85404-469-6</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=bookitem&rft.atitle=Some+Notes+on+the+Early+Development+of+Models+of+Bonding+in+Olefin-Metal+Complexes&rft.btitle=Modern+Coordination+Chemistry%3A+The+Legacy+of+Joseph+Chatt&rft.pages=103-110&rft.pub=RSC+Publishing&rft.date=2002&rft.isbn=978-0-85404-469-6&rft.aulast=Winterton&rft.aufirst=N.&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DVoBxtPb5zCcC%26pg%3DPA103&rfr_id=info%3Asid%2Fen.wikipedia.org%3AZeise%27s+salt" class="Z3988"></span></span> </li> <li id="cite_note-12"><span class="mw-cite-backlink"><b><a href="#cite_ref-12">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFAstruc2007" class="citation book cs1"><a href="/wiki/Didier_Astruc" title="Didier Astruc">Astruc, Didier</a> (2007). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=aVyfo52-nRsC&pg=PA41"><i>Organometallic Chemistry and Catalysis</i></a>. <a href="/wiki/Springer_Science%2BBusiness_Media" title="Springer Science+Business Media">Springer</a>. pp. 41–43. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-3-540-46128-9" title="Special:BookSources/978-3-540-46128-9"><bdi>978-3-540-46128-9</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Organometallic+Chemistry+and+Catalysis&rft.pages=41-43&rft.pub=Springer&rft.date=2007&rft.isbn=978-3-540-46128-9&rft.aulast=Astruc&rft.aufirst=Didier&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DaVyfo52-nRsC%26pg%3DPA41&rfr_id=info%3Asid%2Fen.wikipedia.org%3AZeise%27s+salt" class="Z3988"></span></span> </li> <li id="cite_note-13"><span class="mw-cite-backlink"><b><a href="#cite_ref-13">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFSteven_D._Paget2001" class="citation encyclopaedia cs1">Steven D. Paget (2001). "(−)-Dichloro(ethylene)(α-methylbenzylamine)platinum(II)". <i><a href="/wiki/Encyclopedia_of_Reagents_for_Organic_Synthesis" title="Encyclopedia of Reagents for Organic Synthesis">Encyclopedia of Reagents for Organic Synthesis</a></i>. John Wiley & Sons. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1002%2F047084289X.rd119">10.1002/047084289X.rd119</a>. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/0-471-93623-5" title="Special:BookSources/0-471-93623-5"><bdi>0-471-93623-5</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=bookitem&rft.atitle=%28%E2%88%92%29-Dichloro%28ethylene%29%28%CE%B1-methylbenzylamine%29platinum%28II%29&rft.btitle=Encyclopedia+of+Reagents+for+Organic+Synthesis&rft.pub=John+Wiley+%26+Sons&rft.date=2001&rft_id=info%3Adoi%2F10.1002%2F047084289X.rd119&rft.isbn=0-471-93623-5&rft.au=Steven+D.+Paget&rfr_id=info%3Asid%2Fen.wikipedia.org%3AZeise%27s+salt" class="Z3988"></span></span> </li> </ol></div></div> <div class="navbox-styles"><style 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href="/wiki/Template_talk:Platinum_compounds" title="Template talk:Platinum compounds"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Platinum_compounds" title="Special:EditPage/Template:Platinum compounds"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Platinum_compounds" style="font-size:114%;margin:0 4em"><a href="/wiki/Platinum_compounds" class="mw-redirect" title="Platinum compounds">Platinum compounds</a></div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%">Pt(−II)</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/w/index.php?title=Caesium_platinide&action=edit&redlink=1" class="new" title="Caesium platinide (page does not exist)">Cs<sub>2</sub>Pt</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Pt(0)</th><td class="navbox-list-with-group navbox-list navbox-even hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Tetrakis(triphenylphosphine)platinum(0)" title="Tetrakis(triphenylphosphine)platinum(0)">Pt(PPh<sub>3</sub>)<sub>4</sub></a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Pt(II)</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Carboplatin" title="Carboplatin">Pt(NH<sub>3</sub>)<sub>2</sub>(CO<sub>2</sub>)<sub>2</sub>C<sub>4</sub>H<sub>6</sub></a></li> <li><a href="/wiki/Cisplatin" title="Cisplatin"><i>cis</i>-Pt(NH<sub>3</sub>)<sub>2</sub>Cl<sub>2</sub></a></li> <li><a href="/wiki/Transplatin" title="Transplatin"><i>trans</i>-Pt(NH<sub>3</sub>)<sub>2</sub>Cl<sub>2</sub></a></li> <li><a href="/wiki/Krogmann%27s_salt" title="Krogmann's salt">K<sub>2</sub>Pt(CN)<sub>4</sub></a></li> <li><a href="/wiki/Magnus%27s_green_salt" title="Magnus's green salt">Pt(NH<sub>3</sub>)<sub>4</sub>PtCl<sub>4</sub></a></li> <li><a href="/wiki/Nedaplatin" title="Nedaplatin">Pt(NH<sub>3</sub>)<sub>2</sub>CO<sub>2</sub>CH<sub>2</sub>O</a></li> <li><a href="/wiki/Oxaliplatin" title="Oxaliplatin">(Cy(NH<sub>2</sub>)<sub>2</sub>)PtC<sub>2</sub>O<sub>4</sub></a></li> <li><a href="/wiki/Picoplatin" title="Picoplatin">NH<sub>3</sub>PtCl<sub>2</sub>(PyrMe)</a></li> <li><a href="/wiki/Platinum(II)_acetate" title="Platinum(II) acetate">Pt(OAc)<sub>2</sub></a></li> <li><a href="/wiki/Platinum(II)_bromide" title="Platinum(II) bromide">PtBr<sub>2</sub></a></li> <li><a href="/wiki/Platinum(II)_chloride" title="Platinum(II) chloride">PtCl<sub>2</sub></a></li> <li><a href="/wiki/Platinum(II)_fluoride" title="Platinum(II) fluoride">PtF<sub>2</sub></a></li> <li><a href="/wiki/Platinum(II)_iodide" title="Platinum(II) iodide"><span class="chemf nowrap">PtI<span class="nowrap"><span style="display:inline-block;margin-bottom:-0.3em;vertical-align:-0.4em;line-height:1em;font-size:80%;text-align:left"><sup style="font-size:inherit;line-height:inherit;vertical-align:baseline"></sup><br /><sub style="font-size:inherit;line-height:inherit;vertical-align:baseline">2</sub></span></span></span></a></li> <li><a href="/wiki/Platinum_diphosphide" title="Platinum diphosphide"><span class="chemf nowrap">PtP<sub class="template-chem2-sub">2</sub></span></a></li> <li><a href="/wiki/Potassium_tetrachloroplatinate" title="Potassium tetrachloroplatinate">K<sub>2</sub>PtCl<sub>4</sub></a></li> <li><a href="/wiki/Triplatin_tetranitrate" title="Triplatin tetranitrate">[(PtCl(NH<sub>3</sub>)<sub>2</sub>(C<sub>6</sub>H<sub>12</sub>(NH<sub>2</sub>)<sub>2</sub>))Pt(NH<sub>3</sub>)<sub>2</sub>](NO<sub>3</sub>)<sub>4</sub></a></li> <li><a href="/w/index.php?title=Platinum(II)_hydroxide&action=edit&redlink=1" class="new" title="Platinum(II) hydroxide (page does not exist)">Pt(OH)<sub>2</sub></a></li> <li><a href="/wiki/Platinum-samarium" class="mw-redirect" title="Platinum-samarium">PtSm</a></li> <li><a href="/wiki/Platinum(II)_bis(acetylacetonate)" title="Platinum(II) bis(acetylacetonate)">Pt(C<sub>5</sub>H<sub>7</sub>O<sub>2</sub>)<sub>2</sub></a></li> <li><a href="/wiki/Platinum(II)_sulfide" title="Platinum(II) sulfide">PtS</a></li></ul></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th id="Organoplatinum(II)_compounds" scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Organoplatinum" class="mw-redirect" title="Organoplatinum">Organoplatinum</a>(II) compounds</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <li><a href="/wiki/Dichloro(cycloocta-1,5-diene)platinum(II)" title="Dichloro(cycloocta-1,5-diene)platinum(II)">PtCl<sub>2</sub>(Cod)</a></li> <li><a href="/wiki/Platinum_fulminate" title="Platinum fulminate">Pt(CNO)<sub>2</sub></a></li> <li><a class="mw-selflink selflink">KPtCl<sub>3</sub>C<sub>2</sub>H<sub>4</sub></a></li> </div></td></tr></tbody></table><div> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Pt(IV)</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Adams%27_catalyst" title="Adams' catalyst">PtO<sub>2</sub></a></li> <li><a href="/wiki/Ammonium_hexachloroplatinate" title="Ammonium hexachloroplatinate">(NH<sub>4</sub>)<sub>2</sub>PtCl<sub>6</sub></a></li> <li><a href="/wiki/Chloroplatinic_acid" title="Chloroplatinic acid">H<sub>2</sub>PtCl<sub>6</sub></a></li> <li><a href="/wiki/Platinum(IV)_bromide" title="Platinum(IV) bromide">PtBr<sub>4</sub></a></li> <li><a href="/wiki/Platinum(IV)_chloride" title="Platinum(IV) chloride">PtCl<sub>4</sub></a></li> <li><a href="/wiki/Platinum_tetrafluoride" title="Platinum tetrafluoride">PtF<sub>4</sub></a></li> <li><a href="/wiki/Potassium_hexachloroplatinate" title="Potassium hexachloroplatinate">K<sub>2</sub>PtCl<sub>6</sub></a></li> <li><a href="/wiki/Satraplatin" title="Satraplatin">Pt(OAc)<sub>2</sub>Cl<sub>2</sub>(NH<sub>3</sub>)(NH<sub>2</sub>Cy)</a></li> <li><a href="/wiki/Sodium_hexachloroplatinate" title="Sodium hexachloroplatinate">Na<sub>2</sub>PtCl<sub>6</sub></a></li> <li><a href="/w/index.php?title=Platinum(IV)_hydroxide&action=edit&redlink=1" class="new" title="Platinum(IV) hydroxide (page does not exist)">Pt(OH)<sub>4</sub></a></li> <li><a href="/wiki/Platinum(IV)_iodide" title="Platinum(IV) iodide"><span class="chemf nowrap">PtI<sub class="template-chem2-sub">4</sub></span></a></li> <li><a href="/wiki/Platinum(IV)_sulfide" class="mw-redirect" title="Platinum(IV) sulfide">PtS<sub>2</sub></a></li> <li><a href="/wiki/Platinum_diselenide" title="Platinum diselenide">PtSe<sub>2</sub></a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Pt(V)</th><td class="navbox-list-with-group navbox-list navbox-even hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Platinum_pentafluoride" title="Platinum pentafluoride">PtF<sub>5</sub></a></li> <li><a href="/wiki/Dioxygenyl_hexafluoroplatinate" title="Dioxygenyl hexafluoroplatinate">O<sub>2</sub>PtF<sub>6</sub></a></li> <li><a href="/wiki/Xenon_hexafluoroplatinate" title="Xenon hexafluoroplatinate">XePtF<sub>6</sub></a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Pt(VI)</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Platinum_hexafluoride" title="Platinum hexafluoride">PtF<sub>6</sub></a></li></ul> </div></td></tr></tbody></table></div>    </div><noscript><img src="https://login.wikimedia.org/wiki/Special:CentralAutoLogin/start?type=1x1&useformat=desktop" alt="" 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