Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Brian S. Hammes"'
Publikováno v:
Inorganic chemistry. 40(18)
The tripodal ligand N[CH2CH2NHC(O)NHC(CH3)3]3 ([H6 1]) was used to synthesize a series of monomeric complexes with terminal hydroxo ligands. The complexes [CoII/IIIH3 1(OH)]2-/1-, [FeII/IIIH3 1(OH)]2-/1- , and [ZnIIH3 1(OH)]2- have been isolated and
Publikováno v:
Inorganic Chemistry Communications. 8:513-516
A neutral 1-D supramolecular array containing [Mn(H2)2] building blocks was synthesized by the selective deprotonation of two coordinated imidazole moieties from the cationic Mn(II) complex, [Mn(H22)2]2+. Upon deprotonation the redox potential of [Mn
Publikováno v:
Inorganic Chemistry. 43:7800-7806
Four new Mo(VI)-dioxo complexes of a family of N2X heteroscorpionate ligands are reported which, together with data already available for (TpR)-, provide a unique example of a comprehensive set of isostructural, isoelectronic complexes differing only
Autor:
Victor N. Nemykin, Brian S. Hammes, Balwant S. Chohan, Brian W. Kail, Partha Basu, Carl J. Carrano
Publikováno v:
Inorganic Chemistry. 42:5999-6007
We have previously demonstrated that the complex [(L1O)MoOCl(2)], where L1OH = (2-hydroxy-3-tert-butyl-5-methylphenyl)bis(3,5-dimethylpyrazolyl)methane, exists as both cis and trans isomers (Kail, B.; Nemykin, V. N.; Davie, S. R.; Carrano, C. J.; Ham
Autor:
Zahida Shirin, Brian S. Hammes, Matthew T. Kieber-Emmons, Lev N. Zakharov, Arnold L. Rheingold, Joseph A Letizia, Carl J. Carrano
Publikováno v:
Inorganica Chimica Acta. 346:227-238
The syntheses and characterization of a series of zinc complexes containing the tripodal ligand bis(5-tert-butyl-3-methylpyrazol-2-yl)acetic acid (H2) which is designed to model the 2-His-1-carboxylate facial triad observed in the active sites of var
Publikováno v:
Journal of Chemical Crystallography. 33:431-436
Reaction of the Zn, Cd, or Co nitrate salts with the deprotonated ligand (2-hydroxy-3-t-butyl-methylphenyl)bis(3,5-dimethylpyrazolyl)methane (L1O−) in methanol produced the following complexes: [(L1OH)Zn(NO3)2] in two isomorphs, a = 40.983(8) A, b
Publikováno v:
Inorganica Chimica Acta. 341:33-38
As models for the labile water ligands so ubiquitous in zinc metalloprotein active sites, aquo and hydroxo complexes of zinc with the ester substituted trispyrazolylborate ligand, [(TpCO2Et,Me) have been isolated and crystallographically characterize
Publikováno v:
Journal of the Chemical Society, Dalton Transactions. :3374-3380
The water molecules in complexes [TpCO2Et,MeM(H2O)3]+ where M = Ni, Co, Mn, or Cu(II) are easily displaced by neutral bidentate ligands, L to produce species of the type [TpCO2Et,MeM(L)H2O]+. Attempted deprotonation of the water molecules in the pare
Publikováno v:
Journal of the Chemical Society, Dalton Transactions. :1448-1451
The hydrogen-bond accepting ligand K[TpCO2Et,Me] was prepared and its complexes with divalent Ni, Co, Mn and Cu reveal a stabilization of penta- or hexa-coordinate metal aquo complexes of the general form [TpCO2Et,MeM(H2O)x] (x = 2 or 3) which are un
Autor:
Carl J. Carrano, Brian S. Hammes
Publikováno v:
Inorganica Chimica Acta. :427-433
The Zn(II)CH3 complexes of the heteroscorpionate ligands (3-tert-butyl-2-hydroxy(or thio)-5-methylphenyl)bis(3,5-dimethylpyrazolyl)methane, L1OH or L2SH react with pentafluorothiophenol (HSPhF5). For [(L1O)ZnCH3], this resulted in the formation of