Surface organometallic chemistry of titanium:: Synthesis, characterization, and reactivity of (Si-O)nTi(CH2C(CH3)3)4-n (n = 1, 2) grafted on aerosil silica and MCM-41

被引:34
作者
Bini, Fabien
Rosier, Cecile
Saint-Arroman, Romain Petroff
Neumann, Eva
Dablemont, Celine
de Mallmann, Aimery
Lefebvre, Frederic
Niccolai, Gerald P.
Basset, Jean-Marie
Crocker, Mark
Buijink, Jan-Karel
机构
[1] ENSCPE Lyon, CNRS, UMR 9986, Lab Chim Organomet Surface, F-69616 Villeurbanne, France
[2] Shell Int Chem, Shell Res & Technol Ctr Amsterdam, NL-1030 BN Amsterdam, Netherlands
关键词
D O I
10.1021/om050675g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of tetrakisneopentyl titanium, TiNp4 (1), with the surface of partially dehydroxylated Aerosil silica and MCM-41 and the reactivity of the resultant supported titanium alkyl product with water, alcohols, and oxygen are reported. Two methods of preparation have been investigated and compared for the grafting of TiNp4: (i) reaction of the support with the vapor of the sublimed complex and (ii) impregnation of the support with a solution of the complex. The second method appeared to be more reliable for "larger scale" preparations. The surface species thus obtained were characterized by infrared spectroscopy, solid state NMR, XAFS, elemental analysis, and various test reactions. Whereas on an Aerosil silica partially dehydroxylated at 500 degrees C, SiO2-(500), the surface complex is a monopodal titanium trisalkyl complex, SiO-Ti[CH2C(CH3)(3)](3), 2a, a bipodal titanium bisalkyl complex, ( SiO)(2)Ti[CH2C- CH3)(3)](2), 2b, is obtained as the major species (ca. 65%) with 2a on MCM-41((500)). The reason for this difference in behavior is discussed on the basis of the surface structure. The results obtained from hydrolysis confirmed the structure proposed for the supported alkyl complexes. For the reaction of the alkyl surface complexes with alcohols (MeOH, EtOH, (BuOH)-Bu-t), the surface compounds obtained were characterized by the same techniques and by XPS and UV-vis. The results are consistent with the formation of monosiloxytrisalkoxy titanium complexes on SiO2-(500), SiO-Ti(OR)(3), 3a(OR), and of SiO-Ti((OBu)-Bu-t)(3), 3a(OtBu), and ( SiO)(2)Ti((OBu)-Bu-t)(2), 3b(OtBu), on MCM-41((500)), after reaction with (BuOH)-Bu-t. The supported titanium alkyl, 2a, also reacts with oxygen, leading mainly to SiO-Ti[OCH2C(CH3)(3)](3), probably via an unstable surface compound such as SiO-Ti[OCH2C(CH3)(3)](2)[OOCH2C(CH3)(3)], resulting from the incorporation of two molecules of oxygen in 2a.
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页码:3743 / 3760
页数:18
相关论文
共 95 条
[1]   Modelling the active sites of heterogeneous titanium epoxidation catalysts using titanium silasequioxanes: Insight into specific factors that determine leaching in liquid-phase processes [J].
Abbenhuis, HCL ;
Krijnen, S ;
vanSanten, RA .
CHEMICAL COMMUNICATIONS, 1997, (03) :331-332
[2]   Surface organometallic chemistry of zirconium.: Chemical reactivity of the Si-O-ZrNP3 surface complex synthesized on dehydroxylated silica and application to the modification of mordenite [J].
Adachi, M ;
Nédez, C ;
Wang, XX ;
Bayard, F ;
Dufaud, V ;
Lefebvre, F ;
Basset, JM .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2003, 204 (204-205) :443-455
[3]   Thermolysis of silica-supported bis(neopentyl) complexes of titanium and zirconium [J].
Alladin, T ;
Beaudoin, MC ;
Scott, SL .
INORGANICA CHIMICA ACTA, 2003, 345 :292-298
[4]   Activities and stabilities of heterogeneous catalysts in selective liquid phase oxidations: recent developments [J].
Arends, IWCE ;
Sheldon, RA .
APPLIED CATALYSIS A-GENERAL, 2001, 212 (1-2) :175-187
[5]   ZIEGLER-NATTA CATALYSIS .3. STEREOSPECIFIC POLYMERIZATION OF PROPENE WITH THE CATALYST SYSTEM TICL3-ALET3 [J].
ARLMAN, EJ ;
COSSEE, P .
JOURNAL OF CATALYSIS, 1964, 3 (01) :99-104
[6]   XANES AND EXAFS STUDY OF TITANIUM ALKOXIDES [J].
BABONNEAU, F ;
DOEUFF, S ;
LEAUSTIC, A ;
SANCHEZ, C ;
CARTIER, C ;
VERDAGUER, M .
INORGANIC CHEMISTRY, 1988, 27 (18) :3166-3172
[7]   On the structure and coordination of the oxygen-donating species in Ti↑MCM-41/TBHP oxidation catalysts:: a density functional theory and EXAFS study [J].
Barker, CM ;
Gleeson, D ;
Kaltsoyannis, N ;
Catlow, CRA ;
Sankar, G ;
Thomas, JM .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2002, 4 (07) :1228-1240
[8]   REEVALUATION OF X-RAY ATOMIC ENERGY LEVELS [J].
BEARDEN, JA ;
BURR, AF .
REVIEWS OF MODERN PHYSICS, 1967, 39 (01) :125-&
[9]   A NEW FAMILY OF MESOPOROUS MOLECULAR-SIEVES PREPARED WITH LIQUID-CRYSTAL TEMPLATES [J].
BECK, JS ;
VARTULI, JC ;
ROTH, WJ ;
LEONOWICZ, ME ;
KRESGE, CT ;
SCHMITT, KD ;
CHU, CTW ;
OLSON, DH ;
SHEPPARD, EW ;
MCCULLEN, SB ;
HIGGINS, JB ;
SCHLENKER, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (27) :10834-10843
[10]  
BELLUSSI G, 1994, STUD SURF SCI CATAL, V85, P177