王中夏
(1) 金属有机化合物的合成和反应;(2) 金属有机化合物催化碳-杂原子键活化和官能化;(3) 金属有机化合物催化环酯开环聚合研究。
个性化签名
- 姓名:王中夏
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学术头衔:
博士生导师
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学科领域:
有机化学
- 研究兴趣:(1) 金属有机化合物的合成和反应;(2) 金属有机化合物催化碳-杂原子键活化和官能化;(3) 金属有机化合物催化环酯开环聚合研究。
王中夏,男,中国科技大学化学系教授,博士生导师。1983年在南开大学化学系毕业获学士学位,1986年在南开大学获硕士学位。1986年7月至1993年8月在中国科技大学先后任助教、讲师。1993年8月至1996年10月英国Sussex大学博士研究生,1997年1月获博士学位。1996年12月起任中国科技大学副教授。1999年10月至2000年10月在香港中文大学访问研究。2000年10月起任中国科技大学教授,2001年5月起任中国科技大学博士生导师。研究兴趣:(1) 金属有机化合物的合成和反应;(2) 金属有机化合物催化碳-杂原子键活化和官能化;(3) 金属有机化合物催化环酯开环聚合研究。迄今已主持10余项国家和省、部科学基金,在国内外核心刊物发表论文60余篇。
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王中夏, Zhong-Xia Wang * and Ye-Xin Li
Organometallics 2003, 22, 4900-4904,-0001,():
-1年11月30日
Reaction of Ph2P(8-CH2C9H6N)=NBut (1) with 2 equiv of AlMe3 in toluene under reflux conditions afforded aluminum iminophosphorano(2-methyl-8-quinolyl)methandiide complex (2). The reaction proceeded via the intermediates of a coordination complex, [(AlMe3){Ph2P-(8-CH2C9H6N)=NBut}] (3), and then an addition complex (4) of AlMe3 to the carbon-nitrogen double bond of the quinolyl ring of the neutral ligand. The coordination complex was converted to the singly deprotonated complex [(AlMe2){CH(8-C9H6N)(Ph2P=NBut)}] (5) at 60℃, which further reacted with AlMe3 in toluene under reflux conditions to yield aluminum iminophosphorano (8-quinolyl) methandiide (6). The structures of complexes 2, 4, and 6 were proved by single-crystal X-ray diffraction techniques, and the five-coordinate complexes 3 and 5 were characterized by 27Al NMR spectroscopy.
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【期刊论文】Synthesis of Bisgermavinylidene and Its Reaction with Chalcogens
王中夏, Wing-Por Leung, * Cheuk-Wai So, Zhong-Xia Wang, Jin-Zhi Wang, and Thomas C. W. Mak
Organometallics 2003, 22, 4305-4311,-0001,():
-1年11月30日
The lithium complex [HC(PPh2=NSiMe3)2Li(THF)] (2) prepared by the reaction of BunLi with bis (iminophosphorano) methane reacts with GeCl2·dioxane in different stoichiometric ratios to afford [HC(PPh2=NSiMe3)2GeCl] (3) and [(Me3SiN=PPh2)2C=Ge→Ge=C(PPh2=NSiMe3)2] (4), respectively. Bisgermavinylidene 4 can also be obtained by the reaction of 3 with [Ge{N(SiMe3)2}2] or 2. Further reaction of 4 with Me3NO afforded [(μ-N=Ph2P)(Me3-SiN=Ph2P)C=Ge(OSiMe3)]2 (5), and direct reaction of elemental chalcogens (sulfur, selenium, and tellurium) with 4 afforded [(Me3SiN=PPh2)2C=Ge(μ-E)]2 [E=S (6), Se (7), and Te (8)]. X-ray structures of compounds 2-8 have been determined.
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王中夏, Zhong-Xia Wang * and Ye-Xin Li
Organometallics 2002, 21, 4641-4647,-0001,():
-1年11月30日
Reaction of PhaP(C≡CBut)=NSiMe3 (1) with KP(H)Ph afforded 3-(iminophosphorano)-l-phosphaallyl potassium, [K{P(Ph)C(But)=C(H)P(Ph)a=NSiMe3}(OEta)3] [3·(OEta)3], which was recrystallized from EtaO to give a solvent-free complex, [K{P(Ph)C(But)=C(H)P(Ph)a=N-SiMe3}]∞ (3). Treatment of MeaP(C≡CPh)=NSiMe3 (2) with LiP(R)Ph (R=H, SiMeaBut) formed 2-(iminop hosp horano)-1-phosp haallyllithium, [Li{P(Ph)C{=C(R)Ph}P(Me)a=NSiMe3}-(THE)n] (R=H, n=1.5, 4; R=SiMeaBut, n=2, 5), via a hydrogen or SiMeaBut group 1,3-P→C migration. Reaction of 4 or 5 with SnCla in 2:1 ratio in EtaO yielded P, N-chelatingtin(II) complexes [Sn{P(Ph)C{=C(R)Ph}P(Me)a=NSiMe3}a] (R=H, 6; R=SiMeaBut, 7). Complex 6 was also obtained by treatment of C1SnN(SiMe3)2 with 1 equiv of 4. X-ray data are provided for 3, 5, and 6. Complex 3 is polymeric in the solid state without coordinated solvent molecules, whereas both crystalline 5 and 6 are monomeric.
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王中夏, Zhong-Xia Wang a, *, Da-Qi Wang b, Jian-Min Dou b
Journal of Organometallic Chemistry 665(2003)205-213,-0001,():
-1年11月30日
Reaction of MP(Ph)SiMe2But(M=Li, K) with an equivalent of PhCN afforded the 1-aza-3-phosphaallyllithium and-potassium complexes [M{P(Ph)C(Ph)NSiMeBut}(L)]2(1,M=THF;2, M=K, L=Et2O), respetively. Exposing 2 in vacuo at room temperature, the solvent-free complex [K{P(Ph)C(Ph)NSiMe2But}] (3) was obtained. Treatment of 1 with SnCl2 in 2:1 ratio funished the homoleptic tin (Ⅱ) comples [Sn{P(Ph)C(Ph)NSiMe2But}2] (4). Compound 1 reacted with an equimolar amount of C1SnN(SiMe3)2 to give [P(Ph)C(Ph)=NsiMe2But}]2 (5) via ligand coupling. Reaction of 3 with PhCN produced [K{P(Ph)C(Ph)NC(Ph)NSiMe2But}](6) by addition of the nitrogen atom to PhCN followed of 3 with PhCN produced [K{P(Ph)C(Ph)NC(Ph)NSiMe2But}] (6) by addition of the nitrogen atom th PhCN followed by a 1,3-N→N' migration of the SiMe2But group. Structures of compounds 1,2,4 and 5 have been determinded bysingle crystal X-ray diffraction techniques. The complexes 1 and 2 are dimeric and 4 is both monomeric, while 5 is the product of ligand coupling with formation of new P-P bond.
1-aza-3-Phosphaallyl ligand, Lithium, Potassium, Tin, Complexes, Structures
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王中夏, Wing-Por Leung, * Zhong-Xia Wang, Hung-Wing Li, Qing-Chuan Yang, and Thomas C. W. Mak
J. Am. Chem. Soc. 2001, 123, 8123-8124,-0001,():
-1年11月30日
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王中夏
,-0001,():
-1年11月30日
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王中夏, Zhong-Xia Wang * and Ye-Xin Li
Inorganic Chemistry, Vol. 41, No.23, 2002,-0001,():
-1年11月30日
Reaction of MCl4 (M=Zr, Hf) with 2 equiv of 2-iminophosphorano-1-phosphaallyl lithium [Li{P(Ph)C(=CHPh)P(Me)2=NSiMe3}-(THF)1.5] (1) affords ligand coupling complexes 3 and 4, respectively, while similar treatment of ZrCl4 with [Li{P(Ph)C(=C(SiMe2But)Ph)P(Me)2=NSiMe3}(THF)2] (2) yields ligand transfer complex 5.
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【期刊论文】Solventless syntheses of pyrazole derivatives†
王中夏, Zhong-Xia Wang * and Hua-Li Qin
Green Chem., 2004, 6, 90-92,-0001,():
-1年11月30日
Solventless condensation of a diketone and a hydrazine in the presence of a catalytic amount of sulfuric acid at room temperature afforded pyrazole derivatives 3a-3i and 4g-4i in high yields. The condensation of 2,4-pentanedione and hydrazides gave similar results, while the reaction between 1-phenylbutane-1,3-dione and hydrazides under the same conditions afforded 4,5-dihydro-5-hydroxypyrazole derivatives 6a and 6b, which can be transformed to 4i (for 6b) or a mixture of 1-acylpyrazole and 3i (4i) (for 6a) by thermolysis in the presence of a catalytic amount of sulfuric acid. Similar reaction of ethyl acetoacetate with phenylhydrazine or hydrazine formed 2-pyrazolin-5-one 8 and 3-pyrazolin-5-one 9, respectively. Reactions of 2,4-dinitrophenylhydrazine with 2,4-pentanedione and ethyl acetoacetate yielded hydrazones 10 and 11, respectively.
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王中夏, Zhong-Xia Wang * and Hua-Li Qin
CHEM. COMMUN., 2003, 2450-2451,-0001,():
-1年11月30日
Reaction of an arylacetylene with an azide in hot water gave 1,4-disubstituted 1,2,3-triazoles in high yields, while similar reaction between a terminal aliphatic alkyne and an azide (except m-nitroazidobenzene) afforded a mixture of regioisomers with the ratio of 1,4-to 1,5-isomers ranging from 3: 1 to 28.6: 1. Reactions of m-nitroazidobenzene with either arylalkynes or aliphatic alkynes formed only 1,4-disubstituted derivatives in excellent yields.
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王中夏, Wing-Por Leung, * Zhong-Xia Wang, Hung-Wing Li, and Thomas C.W. Mak
Angew. Chem. Int. Ed. 2001, 40, No.13,-0001,():
-1年11月30日
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