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Complex Formation of 1,5-Bis(amidomethylsulfonyl)pentane with Copper(II) and Iron(III)
ligand denticity

α,ω-Bis(Hydrazidomethylsulfinyl and Sulfonyl)Alkanes: State in solution and interaction with copper(II) hydrazides of carboxylic acids. In the binuclear complex, all four ligands are bridging and differ

Solvation state of iron(III) in aqueous solutions of dimethyl sulfoxide. Complex formation ability of iron(III) with respect to derivatives of sym-triazine and bis(hydrazinocarbonylmethyl) sulfoxide and 1: 2 compositions; in contrast to the Cu(II) and Ni(II) complexes, in the iron complexes the ligand

Complexes of 1,8-bis(hydrazidomethylsulfonyl)octane and 1,10-bis(hydrazidomethylsulfonyl)decane with copper(II) as polydentate ligands; in the pH range of 4.5–5.0 and with copper(II), they form cationic mono- and binuclear

The Impact of Methyl Substituents on the Ag––O–N+ Coordination Bond Denticity of Pyridine N-Oxide OxygenThe coordination bond (CB) denticities of the N-oxide 7 oxygen in three methyl-substituted pyridine

Solvation state of iron(III) in aqueous solutions of dimethyl sulfoxide. Complex formation ability of iron(III) with respect to derivatives of sym-triazine and bis(hydrazinocarbonylmethyl) sulfoxide and 1: 2 compositions; in contrast to the Cu(II) and Ni(II) complexes, in the iron complexes the ligand

Steric control in the metal-ligand electron transfer of iminopyridine-ytterbocene complexes
5-C5Me5, 1) and iminopyridine ligands (IPy = 2,6-iPr2C6H3NCH(C5H3N-R), R = H (2a), 6-C4H3O (2b), 6-C

(Amido)- and (Chlorido)titanium and -zirconium Complexes Coordinated by ansa-Bis(amidinate) Ligands with a Rigid o-Phenylene Linker by the bis(amidinate) ligands {C6H4-1,2-[NC(tBu)N(2,6-R2C6H3)]2}M(NMe2)2 [M = ZrIV, R = Me (3), R = iPr (4

(Amido)- and (Chlorido)titanium and -zirconium Complexes Coordinated by ansa-Bis(amidinate) Ligands with a Rigid o-Phenylene Linker by the bis(amidinate) ligands {C6H4-1,2-[NC(tBu)N(2,6-R2C6H3)]2}M(NMe2)2 [M = ZrIV, R = Me (3), R = iPr (4

Hydrolysis of Mg(BH4)2 and its coordination compounds as a way to obtain hydrogen and denticity of the ligand directly affects the amount of released diborane. In general, the larger the ligand

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