TY - JOUR AU - Nomura, Mitsushiro AU - Cauchy, Thomas AU - Geoffroy, Michel AU - Adkine, Prashant AU - Fourmigué, Marc TI - [CpNi(dithiolene)] (and Diselenolene) Neutral Radical Complexes PY - 2006 JF - Inorganic Chemistry JA - Inorg. Chem. SN - 0020-1669 VL - 45 IS - 20 SP - 8194 EP - 8204 L1 - http://pubs.acs.org/cgi-bin/article.cgi/inocaj/2006/45/i20/pdf/ic0608546.pdf L2 - http://pubs.acs.org/cgi-bin/article.cgi/inocaj/2006/45/i20/html/ic0608546.html L3 - http://pubs.acs.org/cgi-bin/abstract.cgi/inocaj/2006/45/i20/abs/ic0608546.html L4 - http://www.unige.ch/sciences/chifi/publis/pics/double/ref00836.png M3 - 10.1021/ic0608546 UR - http://dx.doi.org/10.1021/ic0608546 N2 - Various preparations of the neutral radical [CpNi(dddt)] complex (dddt = 5,6-dihydro-1,4-dithiin-2,3-dithiolate) were investigated with CpNi sources, [Cp2Ni], [Cp2Ni](BF4), [CpNi(CO)]2, and [CpNi(cod)](BF4), and dithiolene transfer sources, O=C(dddt), the naked dithiolate (dddt2-), the monoanion of square-planar Ni dithiolene complex (NBu4)[Ni(dddt)2], and the neutral complex [Ni(dddt)2]. The reaction of [CpNi(cod)](BF4) with (NBu4)[Ni(dddt)2] gave the highest yield for the preparation of [CpNi(dddt)] (86%). [CpNi(ddds)] (ddds = 5,6-dihydro-1,4-dithiin-2,3-diselenolate), [CpNi(dsdt)] (dsdt = 5,6-dihydro-1,4-diselenin-2,3-dithiolate), [CpNi(bdt)] (bdt = 1,2-benzenedithiolate), and [CpNi(bds)] (bds = 1,2-benzenediselenolate) were synthesized by the reactions of [Cp2Ni] with the corresponding neutral Ni dithiolene complexes [Ni(ddds)2]2, [Ni(dsdt)2], [Ni(bdt)2], and [Ni(bds)2], respectively. The five, formally NiIII, radical complexes oxidize and reduce reversibly. They exhibit, in the neutral state, a strong absorption in the NIR region, from 1000 nm in the dddt/ddds/dsdt series to 720 nm in the bdt/bds series with ε values between 2500 and 5000 M-1 cm-1. The molecular and solid state structures of the five complexes were determined by X-ray structure analyses. [CpNi(dddt)] and [CpNi(ddds)] are isostructural, while [CpNi(dsdt)] exhibits a closely related structure. Similarly, [CpNi(bdt)] and [CpNi(bds)] are also isostructural. Correlations between structural data and magnetic measurements show the presence of alternated spin chains in [CpNi(dddt)], [CpNi(ddds)], and [CpNi(dsdt)], while a remarkably strong antiferromagnetic interaction in [CpNi(bdt)] and [CpNi(bds)] is attributed to a Cp···Cp face-to-face σ overlap, an original feature in organometallic radical complexes. ID - 836 ER -