648435-79-4Relevant academic research and scientific papers
Syntheses, Characterizations, and Coordination Chemistry of the 10-Vertex Phosphadicarbaboranes 6-R-arachno-6,8,9-PC2B7H 11 and 6-R-arachno-6,5,7-PC2B7H11
Hong, Daewon,Rathmill, Scott E.,Carroll, Patrick J.,Sneddon, Larry G.
, p. 16058 - 16073 (2003)
The 10-vertex phosphadicarbaboranes, 6-R-arachno-6,8,9-PC2B 7H11 (1) (R = Ph 1a or Me 1b) and 6-R-arachno-6,5,7-PC2B7H11 (2) (R = Ph 2a or Me 2b) have been synthesized using in situ dehydrohalogenation reactions of RPCl2 (R = Ph or Me) with the arachno-4,5-C2B 7H13 and arachno-4,6-C2B7H 13 carboranes, respectively. X-ray crystallographic determinations in conjunction with DFT/GIAO/NMR calculations and NMR spectroscopic studies have established that both 1 and 2 have open cage structures based on an icosahedron missing two vertexes. The two isomeric compounds differ in the positions of the carbons and bridging hydrogens on the open face. Studies of the reactions of 2a with BH3·THF, S8, and hydrogen peroxide demonstrated that 2a shows strong donor properties yielding the compounds endo-6-H3B-exo-6-Ph-arachno-6,5,7-PC2B 7H11 (3), endo-6-S-exo-6-Ph-arachno-6,5,7-PC 2B7H11 (4), and endo-6-O-exo-6-Ph-arachno-6,5,7-PC2B7H11 (5) in which the BH3, S, and O substitutents are bonded to an electron lone pair localized at the phosphorus endo-position. The reaction of 2a with an excess of S8 results in the loss of a framework boron to produce the unique open-cage compound μ7,8-{HS(Ph)P}-hypho-7,8-C 2B6H11 (6). 2a also formed the donor complexes cis-(η1-[6-Ph-arachno-6,5,7-PC2B7H 11])2PtBr2 (7) and trans-(η 1-[6-Ph-arachno-6,5,7-PC2B7H 11])2PdBr2 (8) in which the metal fragment is bonded in an η1-fashion at the phosphorus endo-position. In these complexes, 2a is functioning as a two-electron sigma donor to the metals and can thus be considered as an analogue of the PR3 ligands in the classical cis-(PPh3)2PtBr2 and trans-(PPh 3)2PdBr2 coordination complexes. Although 1a did not show the donor properties exhibited by 2a, its dianion 6-Ph-6,8,9-PC2B7H92- (1a 2-) readily formed η4-coordinated complexes with late transition metals including 8-Ph-7-(Ph3P) 2-nido-7,8,10,11-PtPC2B7H9 (9), 7-Ph-11-(η5-C5H5)-nido-11,7,9,10-CoPC 2B7H9 (10), and commo-Ni-(7-Ni-8′ -Ph-nido-8′,10′,11′-PC2B7H 9)(7-Ni-8-Ph-nido-8,10,11-PC2B7H9) (11).
