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Article: Dithiolate and diselenolate complexes [Pt2(μ-ECH2CH{double bond, long}CHCH2E)(PPh3)4]2+ (E = S, Se): Synthesis, characterisation and mass spectrometric formation of the dichalcogenide species [Pt2(μ-E2)(PPh3)4]2+

TitleDithiolate and diselenolate complexes [Pt2(μ-ECH2CH{double bond, long}CHCH2E)(PPh3)4]2+ (E = S, Se): Synthesis, characterisation and mass spectrometric formation of the dichalcogenide species [Pt2(μ-E2)(PPh3)4]2+
Authors
KeywordsPlatinum complexes
Electrospray mass spectrometry
Alkylation reactions
Thiolate complexes
Sulfide complexes
Issue Date2009
Citation
Inorganica Chimica Acta, 2009, v. 362, n. 4, p. 1194-1198 How to Cite?
AbstractThe reactions of [Pt2(μ-E)2(PPh3)4] (E = S, Se) with cis-1,4-dichlorobut-2-ene (cis-ClCH2CH{double bond, long}CHCH2Cl) give the dichalcogenolate complexes [Pt2(μ-ECH2CH{double bond, long}CHCH2E)(PPh3)4]2+; an X-ray structure determination on the thiolate complex was carried out. The complexes give the expected dications in ESI mass spectra recorded at very low cone voltages, but at moderate cone voltages undergo facile fragmentation via a retro-Diels-Alder reaction and loss of 1,3-butadiene, giving the dichalcogenide species [Pt2(μ-E2)(PPh3)4]2+. Analogous species containing bidentate phosphine or arsine ligands have been previously generated electrochemically, and studied theoretically. © 2008 Elsevier B.V. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/219371
ISSN
2023 Impact Factor: 2.7
2023 SCImago Journal Rankings: 0.386
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorDevoy, Sarah M.-
dc.contributor.authorHenderson, William-
dc.contributor.authorNicholson, Brian K.-
dc.contributor.authorHor, T. S Andy-
dc.date.accessioned2015-09-23T02:56:54Z-
dc.date.available2015-09-23T02:56:54Z-
dc.date.issued2009-
dc.identifier.citationInorganica Chimica Acta, 2009, v. 362, n. 4, p. 1194-1198-
dc.identifier.issn0020-1693-
dc.identifier.urihttp://hdl.handle.net/10722/219371-
dc.description.abstractThe reactions of [Pt2(μ-E)2(PPh3)4] (E = S, Se) with cis-1,4-dichlorobut-2-ene (cis-ClCH2CH{double bond, long}CHCH2Cl) give the dichalcogenolate complexes [Pt2(μ-ECH2CH{double bond, long}CHCH2E)(PPh3)4]2+; an X-ray structure determination on the thiolate complex was carried out. The complexes give the expected dications in ESI mass spectra recorded at very low cone voltages, but at moderate cone voltages undergo facile fragmentation via a retro-Diels-Alder reaction and loss of 1,3-butadiene, giving the dichalcogenide species [Pt2(μ-E2)(PPh3)4]2+. Analogous species containing bidentate phosphine or arsine ligands have been previously generated electrochemically, and studied theoretically. © 2008 Elsevier B.V. All rights reserved.-
dc.languageeng-
dc.relation.ispartofInorganica Chimica Acta-
dc.subjectPlatinum complexes-
dc.subjectElectrospray mass spectrometry-
dc.subjectAlkylation reactions-
dc.subjectThiolate complexes-
dc.subjectSulfide complexes-
dc.titleDithiolate and diselenolate complexes [Pt2(μ-ECH2CH{double bond, long}CHCH2E)(PPh3)4]2+ (E = S, Se): Synthesis, characterisation and mass spectrometric formation of the dichalcogenide species [Pt2(μ-E2)(PPh3)4]2+-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.ica.2008.06.005-
dc.identifier.scopuseid_2-s2.0-59649113452-
dc.identifier.volume362-
dc.identifier.issue4-
dc.identifier.spage1194-
dc.identifier.epage1198-
dc.identifier.isiWOS:000263322200023-
dc.identifier.issnl0020-1693-

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