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dc.contributor.authorKaiwar, Sharadaen_US
dc.contributor.authorHsu, Johnen_US
dc.contributor.authorVodacek, Anthonyen_US
dc.contributor.authorYap, Glennen_US
dc.contributor.authorLiable-Sands, Louiseen_US
dc.contributor.authorRheingold, Arnolden_US
dc.contributor.authorPilato, Roberten_US
dc.date.accessioned2007-07-05T14:10:47Zen_US
dc.date.available2007-07-05T14:10:47Zen_US
dc.date.issued1997-05-21en_US
dc.identifier.citationJournal of Inorganic Chemistry 36N11 (1997) 2046-2412en_US
dc.identifier.issn0020-1669en_US
dc.identifier.urihttp://hdl.handle.net/1850/4241en_US
dc.descriptionRIT community members may access full-text via RIT Libraries licensed databases: http://library.rit.edu/databases/
dc.description.abstractThe 2,3-disulfidothienoquinoxaline complexes of Cp2Mo and dppePd and the 2,3-disulfidothienopyridine complexes of Cp2Mo were obtained as products from the S8 oxidation of the corresponding metallo-1,2-enedithiolate complexes. The analogous 2-sulfido-3-oxidothienoquinoxaline complexes of Cp2Ti, Cp2Mo, dppPd, and dppePt were prepared from 1-(quinoxalin-2-yl)-2-bromoethanone and the corresponding polysulfido complex. Both Cp2Mo{S2C10H4N2S} and Cp2Mo{SOC10H4N2S} have been characterized crystallographically. These complexes contain an extended planar ring where the metal is bound to substituents at the 2- and 3-positions of the thiophene ring. The oxidation products of the Cp2Mo derivatives all have EPR g values near 1.98 and 97/95Mo hyperfine of </= 8.5 G. All of the complexes have a visible band assigned to an intraligand transition (IL). The excitation of a room-temperature DMSO solution of dppePt{SOC10H4N2S} leads to an emission at 690 nm with a = 0.005. Lifetime measurements were best fit as the sum of two exponential decays with lifetimes of 6 and 0.3 ns (Refer to PDF file for exact formulas).en_US
dc.description.sponsorshipWe are indebted to the donors of the Petroleum Research Fund, administered by the American Chemical Society (Grant No. 28499-G3), and the Exxon Education Foundation for supporting this work.en_US
dc.language.isoen_USen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.ispartofseriesvol. 36en_US
dc.relation.ispartofseriesno. 11en_US
dc.titleMetallo 2,3-Disulfidothienoquinoxaline, 2,3-Disulfidothienopyridine, and 2-Sulfido-3-oxidothienoquinoxaline complexes: synthesis and characterizationen_US
dc.typeArticleen_US
dc.identifier.urlhttp://dx.doi.org/10.1021/ic961428v


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