%0 Generic %A Hill, Anthony F. %A M. A. McQueen, Caitlin %D 2016 %T Novel Carbon Monochalcogenide Coordination Mode: [Rh2{μ-SeCMo(CO)2(Tp*)}24-cod)2] (Tp* = hydrotris(3,5-dimethylpyrazol-1-yl)borate; cod = cyclo-octa-1,5-diene) %U https://acs.figshare.com/articles/dataset/Novel_Carbon_Monochalcogenide_Coordination_Mode_Rh_sub_2_sub_SeCMo_CO_sub_2_sub_Tp_sub_2_sub_sup_4_sup_cod_sub_2_sub_Tp_hydrotris_3_5_dimethylpyrazol_1_yl_borate_cod_i_cyclo_i_octa_1_5_diene_/2537470 %R 10.1021/om3000086.s001 %2 https://acs.figshare.com/ndownloader/files/4180480 %K Tp %K hydrotri %K Novel Carbon Monochalcogenide Coordination Mode %K Rh %K CSe ligand %K Et 4N %X The reaction of [Et4N]­[Mo­(CSe)­(CO)2(Tp*)] (Tp* = hydrotris­(3,5-dimethylpyrazol-1-yl)­borate) with [Rh2(μ-Cl)24-cod)2] (cod = cyclo-octa-1,5-diene) results in the formation of the tetrametallic complex [Rh2{SeCMo­(CO)2(Tp*)}24-cod)2] in which the CSe ligand adopts a crystallographically confirmed and unprecedented μ3:σ,σ′(Se),σ″(C) coordination mode. %I ACS Publications