
Journal of the Chemical Society, Dalton Transactions p. 1701 - 1707 (1981)
Update date:2022-08-04
Topics:
Ainscough, Eric W.
Bingham, Alistair G.
Brodie, Andrew M.
Husbands, June M.
Plowman, Jeffrey E.
The preparation of the following compounds is described: cis-a strong charge-transfer (c.t.) absorption in the range 400-550 nm, with an intensity about 1200 dm3mol-1cm-1, and weaker d-d bands at ca. 750 nm.By studying the variation in the c.t. absorption energy for this extensive series of compounds, where (a) the phenolate is kept constant and the coligands are varied and (b) the phenolate is varied and the coligands are kept constant, it is concluded that the assignment of the c.t. transition is consistent with a partial transfer of an electron from the p? orbital on the phenolate oxygen to a d?* copper orbital.The c.t. band energies of the complexes are dependent on the nature of the solvent (solvents with low Eτ values lowering the c.t. energy), the basicity and number of coligands and phenolato-groups, and the chelate effect (which raises the energy).From these considerations, and e.s.r. data, it is concluded that the copper sites in copper(II) lactoferrin have a CuN2O2O'2 donor set containing two cis tyrosines, one histidine, and one water in the equatorial plane and possibly one histidine and an oxygen-donor ligand (non-ionized phenol) along the axial direction.
Lanling Hongchuang Flame Retardant Co., Ltd.
Contact:+86-531-68858132
Address:East Huafeichang Road, Cangshan County, Linyi, Shandong, China (Mainland)
Contact:+86-913-2223392
Address:No. 32, Xinanjing Road, Weinan City, Shaanxi Province, 714000, China
Contact:0792-8228321
Address:10TH Floor No.121 binjiang Road Xunyang District
Contact:+86-15850770348
Address:51 OF XIANGFANGCUN ROAD, Nanjing 210002, China
Shandong General Materials Co.,Ltd(Shandong Aoertong Chemical Co., Ltd)
Contact:86-531-88072280
Address:No. 1825 Hualong Road, Licheng District, Jinan, Shandong, China
Doi:10.1021/ja00056a069
(1993)Doi:10.1021/ja046124j
(2004)Doi:10.1016/j.ejmech.2004.06.013
(2004)Doi:10.1007/BF00506045
(1982)Doi:10.1016/j.tet.2005.09.081
(2006)Doi:10.1021/ic049094u
(2004)