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- W2023193741 abstract "A rational synthesis for 5-tert-butyl-3-cyano-1-(1,2,3,5-dithiadiazolyl)benzene, which was first observed from thermal cleavage of the bis-dithiadiazolyl, has been developed. Voltammetry and electron paramagnetic resonance (EPR) spectra for this radical are reported and its X-ray structure is described. Despite the bulky tBu substituent, the cyano supramolecular synthon is still able to maintain links to a single neighbouring sulfur atom of the S2 unit, as previously observed in cyano-substituted dithiadiazolyls. In the η2 complex with CpCr(CO)2, no such interactions are observed; the nitrile group forms a centrosymmetric dimer through weak contacts with the para H atom on the aryl ring of the partner molecule. This behaviour is contrasted to similar complexes of less bulky dithiadiazolyls, where intermolecular interactions are retained in the crystalline lattice." @default.
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- W2023193741 date "2007-06-01" @default.
- W2023193741 modified "2023-09-30" @default.
- W2023193741 title "A tert-butyl/cyano substituted (1,2,3,5-dithiadiazolyl)benzene and η2 π complexes with CpCr(CO)2" @default.
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- W2023193741 doi "https://doi.org/10.1016/j.jorganchem.2006.11.049" @default.
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