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Revision as of 15:44, 6 December 2011 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 445342888 of page Sodium_maleonitriledithiolate for the Chem/Drugbox validation project (updated: '').  Latest revision as of 20:36, 23 May 2024 edit FrescoBot (talk | contribs)Bots1,135,457 editsm Bot: link syntax 
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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid of page ] with values updated to verified values.}}
{{chembox {{chembox
| verifiedrevid = 434542581 | verifiedrevid = 464402200
|ImageFile=Na2mnt'.png | ImageFile=Sodium_maleonitriledithiolate.svg
|ImageSize=200px | ImageSize=200px
| PIN=Disodium (''Z'')-1,2-dicyanoethene-1,2-bis(thiolate)
|IUPACName=sodium cis-1,2-dicyano-1,2-ethylenedithiolate
|OtherNames= sodium mnt sodium maleonitriledithiolate | OtherNames= Sodium mnt sodium maleonitriledithiolate
|Section1= {{Chembox Identifiers |Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 5013443 | ChemSpiderID = 5013443
| InChI = 1/C4H2N2S2.2Na/c5-1-3(7)4(8)2-6;;/h7-8H;;/q;2*+1/p-2/b4-3+;; | InChI = 1/C4H2N2S2.2Na/c5-1-3(7)4(8)2-6;;/h7-8H;;/q;2*+1/p-2/b4-3+;;
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = UIEQIOFOWZBELJ-CZEFNJPISA-L | StdInChIKey = UIEQIOFOWZBELJ-CZEFNJPISA-L
| CASNo= | CASNo=5466-54-6
| CASNo_Ref = {{Cascite|correct|CAS}}<ref>{{cite book |title=Chem Sources U.S.A. |date=2001 |publisher=Directories Publishing Company, Incorporated |isbn=978-0-937020-34-0 |page=535 |url=https://books.google.com/books?id=OxAaAQAAMAAJ |language=en}}</ref>
| PubChem = 6523934
| SMILES = ../C(C#N)=C(/)C#N | PubChem = 6523934
| SMILES = ../C(C#N)=C(/)C#N
}} }}
|Section2= {{Chembox Properties |Section2={{Chembox Properties
| C=4|N=2|Na=2|S=2
| Formula=C<sub>4</sub>N<sub>2</sub>Na<sub>2</sub>S<sub>2</sub>
| Appearance=yellow solid
| MolarMass=186.17 g/mol
| Density=
| Appearance=yellow solid
| Density= | MeltingPtC=
| MeltingPtC= | BoilingPt=
| BoilingPt= | Solubility=
| SolubleOther= Soluble
| Solubility=
| Solvent= ethanol, DMF
| SolubleOther= Soluble
| Solvent= ethanol, DMF
}}
|Section3= {{Chembox Hazards
| MainHazards=
| FlashPt=
| Autoignition=
}}
}} }}
}}

'''Sodium maleonitriledithiolate''' is the ] described by the ] {{chem2|Na2S2C2(CN)2}}. The name refers to the cis compound, structurally related to maleonitrile ({{chem2|(CH(CN))2}}). Maleonitriledithiolate is often abbreviated '''mnt'''. It is a "]", i.e. a chelating alkene-1,2-dithiolate. It is a prototypical ] in ]. Several complexes are known, such as {{chem2|](mnt)2](2−)}}.<ref>{{cite book |last1=Day |first1=Peter |url=https://onlinelibrary.wiley.com/doi/10.1002/3527604383.ch4 |title=Molecular Materials Combining Magnetic and Conducting Properties |last2=Coronado |first2=Eugenio |date=2004-12-14 |publisher=Wiley |isbn=978-3-527-30665-7 |editor-last=Miller |editor-first=Joel S. |edition=1 |pages=105–159 |language=en |doi=10.1002/3527604383.ch4 |editor-last2=Drillon |editor-first2=Marc}}</ref>{{rp|143–146}}
+)2(2−)}}.]]
The salt is synthesized by treating ] with ] to give the cyanodithioformate salt, which eliminates elemental ] in aqueous solution:<ref>{{cite book |last1=Davison |first1=A. |url=https://onlinelibrary.wiley.com/doi/10.1002/9780470132418.ch3 |title=Metal Complexes Derived from cis -1,2-dicyano-1,2-ethylenedithiolate and Bis(Trifluoromethyl)-1,2-dithiete |last2=Holm |first2=R. H. |last3=Benson |first3=R. E. |last4=Mahler |first4=W. |date=January 1967 |publisher=Wiley |isbn=978-0-470-13169-5 |editor-last=Muetterties |editor-first=Earl L. |edition=1 |volume=10 |pages=8–26 |language=en |doi=10.1002/9780470132418.ch3}}</ref>
:{{chem2|8 NaCN + 8 CS2 → 4 Na2S2C2(CN)2 + S8}}

The compound was first described in 1958.<ref>
{{cite journal
| author = G. Bähr and G. Schleitzer
| title = Beiträge zur Chemie des Schwefelkohlenstoffs und Selenkohlenstoffs, II. Die Kondensierende Spontan-Entschwefelung von Salzen und Estern der Cyan-Dithioameisensäure. Freie Cyan-Dithioameisensäure
| journal = ]
| year = 1957
| volume = 90
| pages = 438–443
| doi = 10.1002/cber.19570900322
| issue = 3}}</ref>

==References==
<references/>

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