98482-12-3Relevant academic research and scientific papers
Synthesis and X-Ray Crystal Structure of Bis(tetrahydroborato)-bisdicobalt(I), Co2(BH4)2(Ph2P5PPh2)2*0.5C6H6: a Novel Mode of Tetrahydroborate Co-ordination
Holah, David G.,Hughes, Alan N.,Maciaszek, Stanislaw,Magnuson, Vincent R.
, p. 1308 - 1309 (1983)
The title compound, obtained as one of several intermediates in a complex sequence of reactions involving CoII, NaBH4, and α,ω-bis(diphenylphosphino)alkanes, is isolated as a phosphine-bridged binuclear species in which each of two tetrahydroborato groups also bridges the two CoI units via the previously unknown M-H-BH2-H-M type of linkage; an additional and unexpected feature of the X-ray crystal structure is that one hydrogen atom of each of the two central BH2 groups also acts as a bridging ligand.
Reactions of cobalt(II) with NaBH4 in the presence of bidentate phosphines: Crystal and molecular structures of CoH[Ph2P(CH2)3PPh2] 2·C6H6 and [Co(BH4)[Ph2P(CH2)5PPh 2]]20.5C6H6
Holah, David G.,Hughes, Alan N.,Maciaszek, Stanislaw,Magnuson, Vincent R.,Parker, Kenneth O.
, p. 3956 - 3962 (2008/10/08)
The reactions between Co(II) and NaBH4 in the presence of the phosphines Ph2P(CH2)nPPh2 (n = 2-6) and cis- and trans-Ph2PCH=CHPPh2 lead, through a series of intermediates, to the formation of CoH(phosphine)2 species, except in the case of the trans ligand, where hydrogenation occurs and CoH[Ph2P(CH2)2PPh2]2 is formed. Single-crystal X-ray diffraction studies on CoH[Ph2P(CH2)3PPh2] 2·C6H6 show that the compound crystallizes in the monoclinic space group P21/n, with unit cell parameters a = 13.640 (6) A?, b = 15.794 (5) A?, c = 23.870 (9) A?, β = 101.04 (4)°, V = 5047.2 A?3, Z = 4, and dcalcd = 1.267 g cm-3. The structure converged to a conventional R factor of 0.042 for 4754 observations and showed a five-coordinated Co(I) atom with two chelating phosphines and a hydride group in a distorted-trigonal-bipyramidal arrangement. In addition, with two of the longer chain phosphines (n = 4, 5) it is possible to isolate Co(I)-BH4 species shown, in the case of n = 5, to be [Co-(BH4)[Ph2P(CH2)5PPh 2]]2·0.5C6H6. This compound crystallizes in the triclinic space group P1 with unit cell parameters a = 10.305 (3) A?, b = 14.990 (3) A?, c = 20.343 (5) A?, α = 107.87 (2)°, β = 90.72 (2)°, γ = 105.88 (2)°, V = 2861 (3) A?3, Z = 2, and dcalcd = 1.240 g cm-3. The structure converged to a conventional R factor of 0.052 for 4290 observations. The dimeric species consists of two Co(I) atoms bridged by both phosphine ligands and BH4 ligands in a hitherto unknown way such that each BH4 group chelates to each cobalt using one common hydrogen, leaving one terminal hydrogen uninvolved. Alternatively, the BH4 group can be considered as a tridentate ligand to two cobalt atoms separated by 2.869 (1)A?. The cobalt and boron atoms are almost coplanar, but, since there is no obvious strain in the Co-P(CH2)5P-Co linkages, the steric and electronic requirements of the bridging tetrahydroborate groups apparently dictate the distorted coordination geometry about the Co atoms.
