Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Siu Ming Lee"'
Publikováno v:
Journal of Organometallic Chemistry. 596:36-45
Substitution reactions of [W(CO) 5 (THF)] with the azo-functionalized monopyridyl and dipyridyl ligands, namely, 4-phenylazopyridine L 1 and 4,4′-azopyridine L 2 , readily afford two tungsten carbonyl complexes [W(CO) 5 (NC 5 H 4 NNC 6 H 5
Publikováno v:
Journal of Organometallic Chemistry. 595:70-80
New dimeric η 2 -diyne complexes of cobalt [{Co 2 (CO) 6 } 2 (diyne)] (diyne=Me 3 SiC 2 (C 13 H 8 )C 2 SiMe 3 ( 1 ), Me 3 SiC 2 (C 13 H 6 O)C 2 SiMe 3 ( 2 ), Me 3 SiC 2 (C 4 H 2 S) 2 C 2 SiMe 3 ( 3 ), Me 3 SiC 2 (C 14 H 7 Fc)C 2 SiMe 3 (Fc=ferroceny
Autor:
Siu-Ming Lee, Massimo Marcaccio, Jon A. McCleverty, Leigh H. Rees, NC Harden, John C. Jeffery, Elizabeth R. Humphrey, Michael D. Ward
Publikováno v:
Journal of the Chemical Society, Dalton Transactions. :2417-2426
A UV/VIS/NIR spectroelectrochemical study has been carried out on a series of dinuclear complexes of the type [{Mo(TpMe,Me)(O)Cl}2{µ-OO}], where ‘OO’ denotes a bis-phenolate bridging ligand and TpMe,Me is tris(3,5-dimethylpyrazolyl)hydroborate.
Publikováno v:
Journal of the Chemical Society, Dalton Transactions. :3443-3450
Reaction of the oxo-molybdenum(V) precursor [Mo(TpMe,Me)(O)Cl2] [TpMe,Me hydrotris(3,5-dimethylpyrazol-1-yl)borate] with arylamines RNH2, in the presence of Et3N and air, afforded the oxo(imido)molybdenum(VI) complexes [Mo(O)(TpMe,Me)Cl(NR)] 1 (R = 4
Autor:
Wing Tak Wong, Siu Ming Lee
Publikováno v:
Journal of Cluster Science. 9:417-444
The importance of palladium complexes in catalytic processes is well-demonstrated by its applications in hydrogenation processes in industry. Mixed metal clusters of palladium are of interest as the palladium ion can attain either a 16- or 18-electro
Autor:
Siu-Ming Lee, Wing-Tak Wong
Publikováno v:
Coordination Chemistry Reviews. 164:415-482
Publikováno v:
Journal of Cluster Science. 7:435-453
The reaction of the lightly stablized cluster [Os3(CO)10(NCMe)2] with thiosalicylic acid affords two products [{Os3(CO)10(µ-H}]2SC6H4CO2],1 and [Os3H(CO)10SC6,H4C(O)OOs3H(CO)11],2. Complex 2 undergoes CO dissociation to give1 or fragmentation to giv
Publikováno v:
Journal of Organometallic Chemistry. 510:219-231
The complex [(bipy)Pd(C02Me)2] reacts with [Os3(CO)10(NCMe)2] in a 1 : 1 molar ratio to give [Os6Pd(CO)18(bipy)] (1) with a moderate yield, and the crystal structure of 1 is presented. Complex 1 is separately treated with an excess of iodine and tetr
Autor:
Siu-Ming Lee, Wing Tak Wong
Publikováno v:
Journal of Cluster Science. 7:37-47
The reaction of 2,2'-dithiosalicylic acid with two equivalents of [Os3(CO)10 (CH3CN)] in THF at −78°C yields yellow crystals of [{Os3(CO)10(μ-H)}2 (O2CC6H4S)2] 1 in moderate yield. Hydrogenetaion of 1 in refluxing CHCl3 affords [Os3(CO)1(μ-H)(O2
Publikováno v:
Journal of Organometallic Chemistry. 506:77-84
Two new air-stable triosmium clusters, [HOs 3 (CO) 10 (O 2 CC 5 H 4 FeC 5 H 5 )] ( 1 ) and [{Os 3 H(CO) 10 } 2 (O 2 CC 5 H 4 FeC 5 H 4 CO 2 )] ( 2 ), were obtained from the reaction of the labilized cluster [Os 3 (CO) 10 (CH 3 CN) 2 ] and the corresp