Investigation of [Ni{Me4Bzo2[14]aneN4}]Cl2 catalyzed selective hydroxylation of phenol to catechol by H2O2 in the homogeneous medium

被引:21
作者
Abbo, HS
Titinchi, SJJ
Chand, S
Prasad, R [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Roorkee 247667, Uttar Pradesh, India
[2] Gurkul Kangri Univ, Dept Chem, Haridwar 249404, India
[3] Indian Inst Technol, Dept Chem Engn, Roorkee 247667, Uttar Pradesh, India
关键词
oxidation; N-4-macrocycle; catalyst; phenol; catechol;
D O I
10.1016/j.molcata.2004.04.012
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Chemical and electrochemical conversion of phenol to 1,2-dihydroxy benzene using H2O2 as oxidant was studied in presence of[Ni{Me(4)Bzo(2)[14]aneN(4)}]Cl-2 as homogeneous catalyst. The reaction products were analyzed using gas chromatograph. The phenoxide salt of the complex, [Ni{Me(4)Bzo(2)[14]aneN(4)}](C6H5O)(2) exhibits a new irreversible oxidation wave at E-p.c 0.45 V versus Ag/AgCl, which is unlike that observed in its dichloride salt with E-p.c 0.25 V, and arises due to catalyzed electro-oxidation of the phenoxide counter ions. The chemical oxidation by H2O2 was investigated in presence of different solvents and a predominant formation of catechol was observed over hydroquinone (with molar ratio 9:1). The reaction conditions were optimized, in terms of the effect of reaction temperature, amount of catalyst, H2O2 concentration, phenol concentration, nature and volume of solvent used, reaction time and pH, for the maximum transformation of phenol as well as for better selectivity towards the formation of catechol. (C) 2004 Elsevier B.V All rights reserved.
引用
收藏
页码:125 / 132
页数:8
相关论文
共 29 条
[1]   Benzylic oxidation with H2O2 catalyzed by Mn complexes of N,N′,N"-trimethyl-1,4,7-triazacyclononane:: spectroscopic investigations of the active Mn species [J].
Bennur, TH ;
Sabne, S ;
Deshpande, SS ;
Srinivas, D ;
Sivasanker, S .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2002, 185 (1-2) :71-80
[2]   AROMATIC HYDROXYLATION .7. OXIDATION OF SOME BENZENOID COMPOUNDS BY IRON COMPOUNDS AND HYDROGEN-PEROXIDE WITH THE AROMATIC COMPOUND ACTING AS SUBSTRATE AND SOLVENT [J].
BROOK, MA ;
CASTLE, L ;
SMITH, JRL ;
HIGGINS, R ;
MORRIS, KP .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1982, (06) :687-692
[3]  
BROWN SW, 1991, Patent No. 913323
[4]  
BURROWS CJ, 1990, INCLUSION PHENOM MOL, V5, P199
[5]   Catalytic properties of biomimetic metallomacrocycles intercalated in layered double hydroxides and smectite clay: The importance of edge-site access [J].
Chibwe, M ;
Ukrainczyk, L ;
Boyd, SA ;
Pinnavaia, TJ .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 1996, 113 (1-2) :249-256
[6]   Metal substituted aluminophosphate molecular sieves as phenol hydroxylation catalysts [J].
Dai, PSE ;
Petty, RH ;
Ingram, CW ;
Szostak, R .
APPLIED CATALYSIS A-GENERAL, 1996, 143 (01) :101-110
[7]  
DANOPOULOS AA, 1994, ERDOL KOHLE ERDGAS P, V47, P240
[8]  
Furniss B. S., 1989, Vogel's Textbook of Practical Organic Chemistry, V5th, P395
[9]  
HYTBRECHTS DRC, 1991, CATAL LETT, V8, P273
[10]   Kinetics of reaction of the Fe-II-cyclam complex with H2O2 in acetonitrile and the mechanism of catalyzed epoxidation of cyclohexene [J].
Kist, LT ;
Trujillo, MJF ;
Szpoganicz, B ;
Manez, MA ;
Basallote, MG .
POLYHEDRON, 1997, 16 (21) :3827-3833