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【期刊论文】Cyclopropanation of alkenes catalyzed by metallophthalocyanines
周向葛, Hui-Hua Liu a, Yi Wanga, Yuan-Jie Shub, Xiang-Ge Zhoua, c, ∗, Jiang Wu a, Sheng-Yong Yan a
Journal of Molecular Catalysis A: Chemical 246(2006)49-52,-0001,():
-1年11月30日
Metallophthalocyanines bearing substituents especially electron-withdrawing substituents are found to be efficient catalysts for cyclopropanation of alkenes with EDA. The influences of reaction conditions have been studied, leading to the highest yield of 91% for styrene by using fluorosubstituted ruthenium–phthalocyanine complex.
Cyclopropanation, Metallophthalocyanine, Catalyst, Fluoro-substituted
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周向葛, Zhong-Xia Wang a, *, Hui Zhao a, Zhong-Yuan Zhou b, Xiang-Ge Zhou b
Journal of Organometallic Chemistry 595(2000)158-165,-0001,():
-1年11月30日
The reaction of [{m-h2-C(R1) CHR2}(m-CO)Fe2(CO)6] with (m-S2)Fe2(CO)6 forms (m3-S)2Fe3(CO)9 (1) and:or anionic intermediates [{m-h2-C(R1) CHR2}(m-S){Fe2(CO)6}2(m4-S)] (2) depending on the substituents R1 and R2. The actions of the anionic complexes 2 with alkyl halides, PhN2BF4 and acid chlorides give [m-h2-C(R1) CHR2](m-RS)[Fe2(CO)6]2(m4-S) (R alkyl, Ph or acyl). The structures of (m-h2-CH CHPh](m-CH2 CHCH2S)[Fe2(CO)6]2(m4-S)
Iron, Alkenyl ligand, Bridging-sulfur ligand, Complexes, Synthesis, Structures
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【期刊论文】Synthesis, structure and catalytic properties of Re(I)-NOBIN Schiff base complex
周向葛, Zheng-Kai Li a, Yang Li a, b, Liang Lei a, Chi-Ming Che c, Xiang-Ge Zhou a, *
Inorganic Chemistry Communications 8(2005)307-309,-0001,():
-1年11月30日
The chiral mononuclear complex of Re(I)-NOBIN Schiff base (NOBIN=1-amino-10-hydroxylbinaphthyl) was synthesized via the reaction of Re(CO)5Cl and corresponding tridentate ligand in methanol. The structure analysis reveals that the central metal coordinates with nitrogen atom of imine and oxygen atom of salicylaldehyde form a six-membered ring, while the left uncoordinated phenol group adjacent to the binaphthyl backbone forms a hydrogen bonding with water molecule coordinated with the Re(I) ion. This mononuclear complex shows some catalytic ability in asymmetric epoxidation and aziridination with moderate results
Rhenium complex, NOBIN Schiff base, Chiral, Catalytic property
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【期刊论文】Nitrene transfer reaction catalyzed by substituted metallophthalocyanines
周向葛, Sheng-Yong Yan a, Yi Wanga, Yuan-Jie Shub, Hui-Hua Liu a, Xiang-Ge Zhoua, c, ∗
Journal of Molecular Catalysis A: Chemical 248(2006)148-151,-0001,():
-1年11月30日
Metallophthalocyanines bearing substituents are found to be efficient catalysts for nitrene transfer reactions. Under optimized reaction conditions, aziridination of alkenes and amidation of C H bonds with PhI=NTs by using 3-trifluromethylphenyoxy-substituted phthalocyanine-iron complex led to the highest yields of 90% and 85% for 4-methylstyrene and 4-ethyltoluene, respectively.
Nitrene transfer, Aziridination, Amidation, Catalytic, Metallophthalocyanine
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周向葛, Zhong-Xia Wang a, *, Shao-Bin Miao a, Zhong-Yuan Zhou b, Xiang-Ge Zhou b
Journal of Organometallic Chemistry 601(2000)87-92,-0001,():
-1年11月30日
The reaction of [Et3NH] [(m-RE)(m-CO)Fe2(CO)6] (E S, Se) (1) with aryl azides gives bridging triazenido complexes (m-RE)(mp-R1C6H4N3H)Fe2(CO)6 (2-8) (2, RE ButS, R1 H; 3, RE PhS, R1 H; 4, RE ButS, R1 Cl; 5, RE ButS, R1 MeO; 6, RE PhS, R1 MeO; 7, RE PhSe, R1 H; 8, RE PhSe, R1 Cl). These complexes were characterized by elemental analyses and 1H-NMR and IR spectroscopy. The structure of complex 2, established by single-crystal X-ray diffraction analysis, shows that the triazenido ligand binds to two iron centers in a bridging bidentate fashion.
Iron, Selenium, Sulfur, Triazenido ligand, Complex, Structure
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