Publications
381 results found
Whiteoak CJ, Britovsek GJP, Gibson VC, et al., 2009, Electronic effects in oxo transfer reactions catalysed by salan molybdenum(VI) cis-dioxo complexes, DALTON TRANSACTIONS, Pages: 2337-2344, ISSN: 1477-9226
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- Citations: 51
Nimitsiriwat N, Gibson VC, Marshall EL, et al., 2009, Bidentate salicylaldiminato tin(II) complexes and their use as lactide polymerisation initiators, DALTON TRANSACTIONS, Pages: 3710-3715, ISSN: 1477-9226
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- Citations: 39
Cariou R, Chirinos J, Gibson VC, et al., 2009, 1,3-butadiene polymerization by bis(benzimidazolyl)amine metal complexes: Remarkable microstructural control and a protocol for in-reactor blending of trans-1,4-, cis-1,4-, and cis-1,4-co-1,2-vinylpolybutadiene., Macromolecules (Washington, DC, U. S.), Vol: 42, Pages: 1443-1444, ISSN: 0024-9297
Butadiene polymn. catalysts were obtained by treating CoCl2 or CrCl3(THF)3 with bis(benzimidazol-2-yl)methylamine ligand and the catalysts were used with PPh3 and Me aluminoxane to give polybutadienes with various microstructures and mol. wts. [on SciFinder(R)]
Cariou R, Gibson VC, Tomov AK, et al., 2009, Group 4 metal complexes bearing new tridentate (NNO) ligands: Benzyl migration and formation of unusual C-C coupled products., J. Organomet. Chem., Vol: 694, Pages: 703-716, ISSN: 0022-328X
Group 4 metal complexes bearing new phenoxy(benzimidazolyl)-imine, -amine and -amide ligands have been synthesized. A series of metal chloride derivs. has been prepd. via treatment of MCl4(THF)2 (M = Ti, Zr, Hf) with the in situ generated sodium salt of the (benzimidazolyl)imine phenol 1. Reaction of the pro-ligand 2 with TiCl4(THF)2 afforded the corresponding complex 8 in which the amine proton remains bound to the nitrogen donor. Benzyl complexes of zirconium and hafnium were synthesized via treatment of pro-ligands 1 and 2 with M(CH2Ph)4 precursors. The complexes [NNO]M(CH2Ph)3 (6 M = Zr, 7 M = Hf) were found to undergo benzyl migration from the metal center to the imine carbon of the ligand backbone giving complexes 11 and 12; the migration follows first order kinetics. The reaction of 1 with Ti(NMe2)4 led to the formation of an unusual C-C coupled product in which a new piperazine ring has formed. Complexes 11 and 12 undergo related transformations, leading to analogous C-C coupled products which were characterized by x-ray crystallog. Deuterium labeling expts. were carried out to det. the mechanistic pathway of the reactions. Chloride and benzyl complexes 3-12 were screened as pre-catalysts for olefin polymn. [on SciFinder(R)]
Biagini SCG, Gibson VC, Giles MR, et al., 2008, Copolymerization of Amino Acid and Amino Ester Functionalized Norbornenes via Living Ring-Opening Metathesis Polymerization, JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, Vol: 46, Pages: 7985-7995, ISSN: 0887-624X
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- Citations: 8
Long RJ, Jones DJ, Gibson VC, et al., 2008, Zirconium Complexes Containing Tetradentate O,P,P,O Ligands: Ethylene and Propylene Polymerization Studies, ORGANOMETALLICS, Vol: 27, Pages: 5960-5967, ISSN: 0276-7333
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- Citations: 28
Nimitsiriwat N, Gibson VC, Marshall EL, et al., 2008, The reversible amination of tin(II)-ligated imines: Latent initiators for the polymerization of rac-lactide, INORGANIC CHEMISTRY, Vol: 47, Pages: 5417-5424, ISSN: 0020-1669
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- Citations: 59
Long RJ, Gibson VC, White AJP, 2008, Group 4 metal olefin polymerization catalysts stabilized by bidentate O,P ligands, ORGANOMETALLICS, Vol: 27, Pages: 235-245, ISSN: 0276-7333
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- Citations: 63
Zaher D, Tomov AK, Gibson VC, et al., 2008, Titanium complexes bearing bidentate benzimidazole-containing ligands and their behavior in ethylene polymerization., J. Organomet. Chem., Vol: 693, Pages: 3889-3896, ISSN: 0022-328X
A series of potentially bidentate benzimidazolyl ligands of the type (Bim)CH2D (where Bim = benzimidazolyl and D = NMe2 L1, NEt2 L2, NPri2 L3, OMe L4 and SMe L5) has been reacted with Ti(NMe2)4 to give five- and six-coordinate Ti(IV) complexes of the type [(Bim)CH2D]Ti(NMe2)3 and [(Bim)CH2D]2Ti(NMe2)2, resp. The X-ray structures of [{(Bim)CH2OMe}Ti(NMe2)3], [{(Bim)CH2NMe2}2Ti(NMe2)2] and [{(Bim)CH2OMe}2Ti(NMe2)2] are reported along with an evaluation of their behavior in ethylene polymn. [on SciFinder(R)]
O'Reilly RK, Shaver MP, Gibson VC, et al., 2007, alpha-diimine, diamine, and diphosphine iron catalysts for the controlled radical polymerization of styrene and acrylate monomers, MACROMOLECULES, Vol: 40, Pages: 7441-7452, ISSN: 0024-9297
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- Citations: 71
Allan LEN, Shaver MP, White AJP, et al., 2007, Correlation of metal spin-state in alpha-diimine iron catalysts with polymerization mechanism, INORGANIC CHEMISTRY, Vol: 46, Pages: 8963-8970, ISSN: 0020-1669
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- Citations: 60
Gibson VC, Redshaw C, Solan GA, et al., 2007, Aluminum alkyl-mediated route to novel N,N,O-chelates for five-coordinate iron(II) chloride complexes: Synthesis, structures, and ethylene polymerization studies, ORGANOMETALLICS, Vol: 26, Pages: 5119-5123, ISSN: 0276-7333
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- Citations: 47
Shaver MP, Allan LEN, Gibson VC, 2007, Organometallic intermediates in the controlled radical polymerization of styrene by alpha-diimine iron catalysts, ORGANOMETALLICS, Vol: 26, Pages: 4725-4730, ISSN: 0276-7333
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- Citations: 60
Nimitsiriwat N, Gibson VC, Marshall EL, et al., 2007, Tert-butylamidinate tin(II) complexes: high activity, single-site initiators for the controlled production of polylactide, Dalton Transactions
The tin(II) coordination chemistry of two monoanionic N,N-bis(2,6-diisopropylphenyl)alkylamidinate ligands is described. Complexation studies with the acetamidinate, [MeC(NAr)2]–, (Ar = 2,6-iPr2C6H3) are complicated by the side formation of the bis(amidinate) tin(II) compound, [MeC(NAr)2]2Sn, 1. By contrast, the bulkier tert-butylamidinate, [tBuC(NAr)2]–, allows tin(II) mono-halide, -alkoxide and -amide complexes to be isolated cleanly in high yields. Thus, the reaction of [tBuC(NAr)2]H with nBuLi and subsequent treatment with SnCl2 generates [tBuC(NAr)2]SnCl, 2, in ca. 70% yield. Reactions of 2 with LiOiPr, LiNMe2 and LiNTMS2 afford [tBuC(NAr)2]Sn(OiPr), 3, [tBuC(NAr)2]Sn(NMe2), 4, and [tBuC(NAr)2]Sn(NTMS2), 5, respectively. The molecular structures of complexes 1–4 are reported. Complexes 3, 4 and 5 have been investigated as initiators for the ring-opening polymerisation of rac-lactide: 3 and 4 display characteristics of well-controlled polymerisation initiators, but high molecular weight polymer is observed with 5 due to inefficient initiation, a consequence of the steric bulk of the NTMS2 unit. Polymerisations with 3 and 4 are faster than for the corresponding -diketiminate tin(II) complexes, consistent with the more open nature of the tin(II) coordination sphere.
Gibson VC, Redshaw C, Clegg W, et al., 2007, 'Electronic bending' of imido ligands and the effect on the coordination mode of a tridentate ancillary ligand, POLYHEDRON, Vol: 26, Pages: 3161-3167, ISSN: 0277-5387
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- Citations: 5
Gibson VC, Redshaw C, Solan GA, 2007, Bis(imino)pyridines: Surprisingly reactive ligands and a gateway to new families of catalysts, CHEMICAL REVIEWS, Vol: 107, Pages: 1745-1776, ISSN: 0009-2665
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- Citations: 714
Shaver MP, Allan LEN, Gibson VC, 2007, Ethylene polymerization under mild conditions using simple aluminum alkyls and chloro activators, ORGANOMETALLICS, Vol: 26, Pages: 2252-2257, ISSN: 0276-7333
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- Citations: 16
Atkinson RCJ, Gerry K, Gibson VC, et al., 2007, Synthesis of 1,1 '-ferrocenediyl salicylaldimine ligands and their application in titanium-initiated lactide polymerization, ORGANOMETALLICS, Vol: 26, Pages: 316-320, ISSN: 0276-7333
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- Citations: 56
Doyle DJ, Gibson VC, White AJP, 2007, Synthesis and structures of bimetallic and polymeric zinc coordination compounds supported by salicylaldiminato and anilido-aldimine ligands, DALTON TRANSACTIONS, Pages: 358-363, ISSN: 1477-9226
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- Citations: 37
Tang Z, Gibson VC, 2007, rac-Lactide polymerization using aluminum complexes bearing tetradentate phenoxy-amine ligands, EUROPEAN POLYMER JOURNAL, Vol: 43, Pages: 150-155, ISSN: 0014-3057
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- Citations: 65
Redshaw C, Gibson VC, Elsegood MRJ, et al., 2007, New coordination modes at molybdenum for 2-diphenylphosphinoaniline derived ligands, CHEMICAL COMMUNICATIONS, Pages: 1951-1953, ISSN: 1359-7345
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- Citations: 7
Nimitsiriwat N, Gibson VC, Marshall EL, et al., 2007, Mono- versus Bis-chelate Formation in Triazenide and Amidinate Complexes of Magnesium and Zinc., Inorg. Chem., Vol: 46, Pages: 9988-9997, ISSN: 0020-1669
Magnesium and zinc complexes of the monoanionic ligands N,N'-bis(2,6-di-isopropylphenyl)triazenide, L1, N,N'-bis(2,6-di-isopropylphenyl)acetamidinate, L2, and N,N'-bis(2,6-di-isopropylphenyl)tert-butylamidinate, L3, have been synthesized, but only L3 possesses sufficient steric bulk to prevent bis-chelation. Hence, the reaction of L1H with excess ZnEt2 leads to the isolation of (L1)2Zn, 1; L1H also reacts with Bu2Mg in Et2O to afford (L1)2Mg(Et2O), 2. Similar reactivity is obsd. for L2H, leading to the formation of (L2)2Zn, 3, and (L2)2Mg, 4. The reaction of L2H with ZnR2 may also afford the tetranuclear aggregates {(L2)Zn2R2}2O, 5 (R = Me) and 6 (R = Et). By contrast, the tert-butylamidinate ligand was found to exclusively promote mono-chelation, allowing (L3)ZnCl(THF), 7, [(L3)Zn(μ-Cl)]2, 8, (L3)ZnN(SiMe3)2, 9, (L3)MgiPr(Et2O), 10, and (L3)MgiPr(THF), 11, to be isolated. X-ray crystallog. analyses of 1, 2, 3, 4, 5, 6, 8, and 10 indicate that the capacity of L3 to resist bis-chelation is due to greater occupation of the metal coordination sphere by the N-aryl substituents. [on SciFinder(R)]
McTavish S, Britovsek GJP, Smit TM, et al., 2007, Iron-based ethylene polymerization catalysts supported by bis(imino)pyridine ligands: Derivatization via deprotonation/alkylation at the ketimine methyl position., J. Mol. Catal. A: Chem., Vol: 261, Pages: 293-300, ISSN: 1381-1169
Bis(imino)pyridine ligands, L [where L = 2,6-(ArNCR1)2C5H3N R1 = Et, iPr, CH2CH2Ph or CH(CH2Ph)2 and Ar = 2,4,6-(Me)3C6H2 (MES) or 2,6-(iPr)2C6H3 (DIPP)] have been prepd. by deprotonation of the parent ketimine ligand (R1 = Me) using lithium diisopropylamide (LDA), followed by alkylation with the appropriate alkylhalide. The corresponding iron dichloride complexes LFeCl2 are highly active ethylene polymn. catalysts upon treatment with methylaluminoxane (MAO), with activities in the range of 3000-18,000 g/mmol bar h. The mol. wts. (Mn) of the resultant polyethylenes lie in the range of 6500-24,000 with broad mol. wt. distributions (16.5-38.0). The nature of the imine carbon substituent has a marked effect on the polymer mol. wt. whereas the catalyst activity is largely unaffected by changes to this substituent. [on SciFinder(R)]
Hormnirun P, Marshall EL, Gibson VC, et al., 2006, Study of ligand substituent effects on the rate and stereoselectivity of lactide polymerization using aluminum salen-type initiators, PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, Vol: 103, Pages: 15343-15348, ISSN: 0027-8424
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- Citations: 214
O'Reilly RK, Shaver MP, Gibson VC, 2006, Nickel(II) alpha-diimine catalysts for the atom transfer radical polymerization of styrene, INORGANICA CHIMICA ACTA, Vol: 359, Pages: 4417-4420, ISSN: 0020-1693
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- Citations: 17
Dove AP, Gibson VC, Marshall EL, et al., 2006, Synthetic, structural, mechanistic, and computational studies on single-site beta-diketiminate tin(II) initiators for the polymerization of rac-lactide, JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, Vol: 128, Pages: 9834-9843, ISSN: 0002-7863
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- Citations: 199
Gregson CKA, Gibson VC, Long NJ, et al., 2006, Redox control within single-site polymerization catalysts, JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, Vol: 128, Pages: 7410-7411, ISSN: 0002-7863
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- Citations: 253
Jones DJ, Gibson VC, 2006, Facile synthesis of 2-arylpyrroles from 4-oxo-butanoic acids and their use in the preparation of bis(pyrrolyl)methanes, HETEROCYCLES, Vol: 68, Pages: 1121-+, ISSN: 0385-5414
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- Citations: 7
Gibson VC, 2006, Shuttling polyolefins to a new materials dimension, SCIENCE, Vol: 312, Pages: 703-704, ISSN: 0036-8075
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- Citations: 55
Oakes DCH, Gibson VC, White AJP, et al., 2006, Highly active titanium-based olefin polymerization catalysts supported by bidentate phenoxyamide ligands, INORGANIC CHEMISTRY, Vol: 45, Pages: 3476-3477, ISSN: 0020-1669
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- Citations: 30
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