Article ID Journal Published Year Pages File Type
1320820 Journal of Organometallic Chemistry 2015 7 Pages PDF
Abstract

Enantiomerically pure electron rich Cp2Mo(dithiolene) complexes have been synthesized from the enantiopure dithiolene ligands, namely the (R)- and the (S)-3(1-phenylethyl)-1,3-thiazoline-2-thione-4,5-dithiolate ligands. These heteroleptic molybdenum complexes act as very good electron donors, as demonstrated through electrochemical investigations. Both isomers form charge transfer salts with TCNQ with a 1:1 stoechiometry which have been characterized by single crystal X-ray diffraction, EPR and UV–vis spectroscopic investigations. Circular dichroism (CD) experiments were also carried out on the neutral (R) and (S) enantiomers as well as on the mono oxidized species of these Cp2Mo dithiolene complexes.

Graphical abstractThe synthetic approach towards chiral Cp2Mo(R*-thiazdt) complexes, (R* = 1-phenylethyl), and their ability to form charge transfer salts with TCNQ are presented.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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