نتایج جستجو برای: 13 cyclooctadiene
تعداد نتایج: 332763 فیلتر نتایج به سال:
Plant endophytic microorganisms represent a largely untapped resource for new bioactive natural products. Eight polyketide natural products were isolated from a mangrove endophytic fungus Phomosis sp. A818. The structural elucidation of these compounds revealed that they share a distinct feature in their chemical structures, an oxygen-bridged cyclooctadiene core skeleton. The study on their str...
Two novel boron-based flexible scorpionate ligands based on 7-azaindole, Li[HB(azaindolyl)(2)(1-naphthyl)] and Li[HB(azaindolyl)(2)(mesityl)] {Li[(Naphth)Bai] and Li[(Mes)Bai] respectively}, have been prepared (mesityl = 2,4,6-trimethylphenyl). These salts have been isolated in two forms, either as dimeric structures which contain bridging hydride interactions with the lithium centres or as cry...
Isomerization and Hydrogenation of Dimethyl Maleate and 1,5-Cyclooctadiene by Nickel Cyanide Complex
aminocarboxylic acids, such as 2-aminobenzoic acid, react easily with [ir(cod)(pme3)3]cl, (cod=1,5-cyclooctadiene), in thf to produce hydridoaminocarboxylato iridium(iii) complexes in high yields. these octahedral complexes are formed via oxidative addition reaction of the o-h bond of the carboxylic group with the central metal. the starting iridium(i) complex losses the cod molecule, the chlor...
An Ir(I) complex of an acetamidinato ligand was synthesized by reaction of N,N'-diphenylacetamidine, PhN[double bond, length as m-dash]C(Me)NHPh, with either MeLi and [{Ir(cod)}2(μ-Cl)2] or [{Ir(cod)}2(μ-OMe)2] and was characterized by X-ray crystallography as a mononuclear complex, [Ir{PhNC(Me)NPh}(cod)] (1; where cod = 1,5-cyclooctadiene). Reaction of 1 with CO afforded a dinuclear carbonyl c...
In situ labelling and spectroscopic experiments are used to explain the key points in the stabilisation of ruthenium nanoparticles (RuNPs) generated in imidazolium-based ionic liquids (ILs) by decomposition of (eta(4)-1,5-cyclooctadiene)(eta(6)-1,3,5-cyclooctatriene)ruthenium(0), Ru(COD)(COT), under dihydrogen. These are found to be: (1) the presence of hydrides at the RuNP surface and, (2) the...
The reaction of gem-dithiol compounds R 2C(SH) 2 (R = Bn (benzyl), (i) Pr; R 2 = -(CH 2) 4-) with dinuclear rhodium or iridium complexes containing basic ligands such as [M(mu-OH)(cod)] 2 and [M(mu-OMe)(cod)] 2, or the mononuclear [M(acac)(cod)] (M = Rh, Ir, cod = 1,5-cyclooctadiene) in the presence of a external base, afforded the dinuclear complexes [M 2(mu-S 2CR 2)(cod) 2] ( 1- 4). The monod...
The activation of the C≡N moiety in the redox-active metalloligand [CpRu{κ(3)N(pz)-1}][PF6] (2) (1: ambidentate hybrid ligand, N≡C-C(pz)3, with pz = pyrazolyl) was observed in the reaction with [Ir(cod)Cl]2 (cod = 1,5-cyclooctadiene). By performing detailed NMR spectroscopic and X-ray crystallographic investigations the product was found to be a bimetallic Ru(II)-Ir(III) complex of the composit...
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