Journal of the Chemical Society, Dalton Transactions p. 2801 - 2806 (1991)
Update date:2022-08-05
Topics:
Bessel, Carol A.
See, Ronald F.
Jameson, Donald L.
Churchill, Melvyn Rowen
Takeuchi, Kenneth J.
The synthesis, characterization, and crystal structure of trans-a = 14.158(2), c = 14.493(3) Angstroem, and Z = 3.Both the RuII-containing cation and the perchlorate anion (which is disordered) lie on a crystallographic two-fold axis.This represents the first structural characterization of a transition-metal complex which utilizes a member of the family of bis(pyrazolyl)pyridine ligands.In addition, the crystal structure yields evidence that the ligand L may be sterically more suitable for co-ordination to a ruthenium(II) centre than the analogous diphenyl-substituted terpyridine ligand, dpt (6,6''-diphenyl-2,2':6'2''-terpyridine).For both tridentate ligands, the donor nitrogen atoms take up three meridional sites and the phenyl substitutents are directed toward the fourth equatorial co-ordination site; however, due to the large distance between the two phenyl arms of L (relative to the dpt), the former ligand can be utilized in synthesizing the present ruthenium(II) complex whereas the analogous dpt complex cannot readily be prepared.
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Doi:10.1016/S0040-4020(01)81932-3
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(2012)Doi:10.1016/j.jorganchem.2012.05.042
(2012)Doi:10.1007/s10847-013-0348-4
(2014)Doi:10.1016/0040-4039(91)80568-Q
(1991)Doi:10.1016/0040-4039(91)80573-O
(1991)
