Ligand-tailored single-site silica supported titanium catalysts: Synthesis, characterization and towards cyanosilylation reaction

被引:7
作者
Xu, Wei [1 ]
Li, Yani [1 ]
Yu, Bo [1 ]
Yang, Jindou [1 ]
Zhang, Ying [1 ]
Chen, Xi [1 ]
Zhang, Guofang [1 ]
Gao, Ziwei [1 ]
机构
[1] Shaanxi Normal Univ, MOE Sch Chem & Chem Engn, Key Lab Appl Surface & Colloid Chem, Xian 710062, Peoples R China
基金
中国国家自然科学基金;
关键词
Surface organometallic chemistry; Silica; Surface titanium complex; Cyanosilylation; SURFACE ORGANOMETALLIC CHEMISTRY; HETEROGENEOUS CATALYSTS; MESOPOROUS SILICA; MOLECULAR-SIEVES; ACTIVE-SITES; TI; EPOXIDATION; METATHESIS; OXIDATION; ALKANES;
D O I
10.1016/j.jssc.2014.10.011
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A successive anchoring of Ti(NMe2)(4), cyclopentadiene and a O-donor ligand, 1-hydroxyethylbenzene (PEA), 1,1'-bi-2-naphthol (Binol) or 2,3-dihydroxybutanedioic acid diethyl ester (Tartrate), on silica was conducted by SOMC strategy in moderate conditions. The silica, monitored by in-situ Fourier transform infrared spectroscopy (in-situ FT-IR), was pretreated at different temperatures (200, 500 and 800 degrees C). The ligand tailored silica-supported titanium complexes were characterized by in-situ FT-IR, C-13 CP MAS-NMR, X-ray photoelectron spectroscopy (XPS), X-ray absorption near edge structure (XANES) and elemental analysis in detail, verifying that the surface titanium species are single sited. The catalytic activity of the ligand tailored single-site silica supported titanium complexes was evaluated by a cyanosilylation of benzaldehyde. The results showed that the catalytic activity is dependent strongly on the dehydroxylation temperatures of silica and the configuration of the ligands. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:208 / 215
页数:8
相关论文
共 51 条
[1]   A REEXAMINATION OF THE CHEMISORPTION OF TRIMETHYLALUMINUM ON SILICA [J].
BARTRAM, ME ;
MICHALSKE, TA ;
ROGERS, JW .
JOURNAL OF PHYSICAL CHEMISTRY, 1991, 95 (11) :4453-4463
[2]  
Basset J.-M., 2009, MODERN SURFACE ORGAN
[3]   Preparation, characterization, and performance of tripodal polyphosphine rhodium catalysts immobilized on silica via hydrogen bonding [J].
Bianchini, C ;
Burnaby, DG ;
Evans, J ;
Frediani, P ;
Meli, A ;
Oberhauser, W ;
Psaro, R ;
Sordelli, L ;
Vizza, F .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (25) :5961-5971
[4]   Alkane metathesis catalyzed by a well-defined silica-supported mo imido alkylidene complex:: [(SiO)Mo(=NAr)(=CHtBu)(CH2tBu)] [J].
Blanc, Frederic ;
Coperet, Christophe ;
Thivolle-Cazat, Jean ;
Basset, Jean-Marie .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (37) :6201-6203
[5]   Fast Synthesis of MOF-5 Microcrystals Using Sol-Gel SiO2 Nanoparticles [J].
Buso, Dario ;
Nairn, Kate M. ;
Gimona, Michele ;
Hill, Anita J. ;
Falcaro, Paolo .
CHEMISTRY OF MATERIALS, 2011, 23 (04) :929-934
[6]   A highly active well-defined rhenium heterogeneous catalyst for olefin metathesis prepared via surface organometallic chemistry [J].
Chabanas, M ;
Baudouin, A ;
Copéret, C ;
Basset, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (09) :2062-2063
[7]   Size effects in the Raman spectra of TiO2 nanoparticles [J].
Choi, HC ;
Jung, YM ;
Kim, SB .
VIBRATIONAL SPECTROSCOPY, 2005, 37 (01) :33-38
[8]   Homogeneous and heterogeneous catalysis:: Bridging the gap through surface organometallic chemistry [J].
Copéret, C ;
Chabanas, M ;
Saint-Arroman, RP ;
Basset, JM .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (02) :156-181
[9]   SYNTHESIS OF AN ULTRALARGE PORE TITANIUM SILICATE ISOMORPHOUS TO MCM-41 AND ITS APPLICATION AS A CATALYST FOR SELECTIVE OXIDATION OF HYDROCARBONS [J].
CORMA, A ;
NAVARRO, MT ;
PARIENTE, JP .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1994, (02) :147-148
[10]  
Dal V., 2010, MOLECULES, V15, P3829