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pro vyhledávání: '"Tony Hascall"'
Carbene-induced rearrangement of 8,8-dibromobicyclo[5.1.0]octa-2,4-dienes and subsequent in situ deprotonation of the dihydropentalenes formed represents a straightforward and versatile solution route to pentalene ligands for use in organometallic ch
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https://ora.ox.ac.uk/objects/uuid:87d5f70f-8d42-47d1-9c50-5bd881adbfbc
Publikováno v:
Organometallics. 23:3808-3813
Reaction of 1,4-(BBr 2 ) 2 C 6 H 4 with cobaltocene gives a bimetallic cobalt complex with cyclopentadienyl and boratabenzene ligands. Oxidation allows the dicationic dicobalt(III) complex to be isolated; the bis(hexafluorophosphate) salt has been st
Publikováno v:
Journal of Organometallic Chemistry. 652:37-49
Mo(PMe 3 ) 6 reacts with ArOH (Ar=2,4,6-C 6 H 2 Me 3 , 2,6-C 6 H 3 Pr i 2 ) to give coordinatively unsaturated aryloxy-hydride derivatives Mo(PMe 3 ) 4 (OAr)H. The formation of Mo(PMe 3 ) 4 (OAr)H is in marked contrast to the cyclometalated products
Publikováno v:
Inorganic Chemistry. 39:4240-4243
The bis(2-mercapto-1-methylimidazolyl)(pyrazolyl)hydroborato derivatives [pzBmMe]2Zn, [pzBmMe]2Co, and [pzBmMe]2Cd have been isolated and structurally characterized by X-ray diffraction. Despite their common [pzBmMe]2M composition, each of these comp
Publikováno v:
Polyhedron. 19:1063-1066
Mo(PMe 3 ) 5 H 2 reacts with catecholborane (CatBH) to give Mo(PMe 3 ) 4 (η 2 -H 2 BCat)H. Structural characterization by X-ray diffraction suggests that the complex is best represented as a borohydride complex, as opposed to a boryl-hydride derivat
Autor:
Clare Kimblin, Tony Hascall, Gerard Parkin, Jeffrey B. Bonanno, Brian M. Bridgewater, Vincent J. Murphy
Publikováno v:
Inorganic Chemistry. 39:967-974
X-ray diffraction studies on a series of cationic divalent metal nitrate complexes supported by the tris(1-isopropyl-4-tert-butylimidazolyl)phosphine ligand, {[PimPri,But]M(NO3)}+ (M = Co, Cu, Zn, Cd, Hg), demonstrate that the nitrate ligand coordina
Publikováno v:
Journal of Organometallic Chemistry. 596:22-26
Magnesium and zinc alkyl complexes supported by the phenyltris(3- t -butylpyrazolyl)borato ligand, [PhTp Bu t ]MgR (R=Me, Et) and [PhTp Bu t ]ZnEt, have been synthesized by reaction of [PhTp Bu t ]Tl with R 2 M (M=Mg, Zn). Comparison of the structure
Publikováno v:
Journal of the Chemical Society, Dalton Transactions. :891-897
Bidentate [S2]-donor bis(mercaptoimidazolyl) ligands, [BmMe]− and [BmMes]−, have been synthesized by reaction of [BH4]− with 2-mercapto-1-methylimidazole and 2-mercapto-1-mesitylimidazole, respectively. Subsequent treatment with ZnX2 (X = Me, I
Publikováno v:
Journal of the Chemical Society, Dalton Transactions. :1267-1274
The bis(mercaptoimidazolyl)(pyrazolyl)hydroborato and tris(mercaptoimidazolyl)hydroborato ligands, [pzBmMe]− and [TmPh]−, have been used to prepare complexes of both thallium(I) and thallium(III), namely [pzBmMe]Tl, [pzBmMe]TlMe2, {[TmPh]2Tl}2 an
Autor:
Tony Hascall, and Richard A. Friesner, Gerard Parkin, Michael D. Beachy, Vincent J. Murphy, Daniel Rabinovich
Publikováno v:
Journal of the American Chemical Society. 121:11402-11417
Experimental observations, together with a theoretical analysis, indicate that the energetics of the oxidative addition of H2 to the six-coordinate molybdenum and tungsten complexes trans-M(PMe3)4X2 (M = Mo, W; X = F, Cl, Br, I) depend very strongly