Supported inorganic oxide

Silica is the most commonly used solid support. Treatment with complexes bearing alkoxy- or chlorosilane functional groups is a common way to generate supported complexes on silica or any inorganic oxide containing surface silanol (Si-OH) groups (Scheme 7.2).23,24... 

The induction of steric effects by the pore walls was first demonstrated with heterogeneous catalysts, prepared from metal carbonyl clusters such as Rh6(CO)16, Ru3(CO)12, or Ir4(CO)12, which were synthesized in situ after a cation exchange process under CO in the large pores of zeolites such as HY, NaY, or 13X.25,26 The zeolite-entrapped carbonyl clusters are stable towards oxidation-reduction cycles this is in sharp contrast to the behavior of the same clusters supported on non-porous inorganic oxides. At high temperatures these metal carbonyl clusters aggregate to small metal particles, whose size is restricted by the dimensions of the zeolitic framework. Moreover, for a number of reactions, the size of the pores controls the size of the products formed thus a higher selectivity to the lower hydrocarbons has been reported for the Fischer Tropsch reaction. 

Heterogeneous reactions facilitated by supported reagents on inorganic oxide surfaces have received attention in recent years, both in the laboratory as well as in industry. Although the first description of the surface-mediated chemical transformation dates back to 1924 [13], it was not until almost half a century later that the technique received extensive attention with the appearance of several reviews, books and account articles [14—22],... 

In contrast to supported homogeneous catalysis, surface organometallic chemistry (SOMC) uses an inorganic oxide (ExOy) as a solid ligand, on which the metal is directly attached by at least a bond with a surface atom, usually an oxygen, through a M-OE bond. 

In a typical inorganic oxide, the oxide surface acquires a charge by the dissociation or adsorption of potential determining ions at specific amphoteric surface groups or sites. As a consequence the equation of state of such surfaces will involve parameters that characterize surface reactions. In addition, one may also allow for the adsorption of anions and cations of the supporting electrolyte. However, in this paper we shall ignore this possibility to keep the discussion clear. Such embellishments of the model of the surface do not alter the key ideas presented here. 

A significant recent advance has been the development of microfiltration and ultrafiltration membranes composed of inorganic oxide materials. These are presently produced by two main techniques (a) deposition of colloidal metal oxide on to a supporting material such as carbon, and (b) as purely ceramic materials by high temperature sintering of spray-dried oxide microspheres. Other innovative production techniques lead to the... 

One advantage of sol-gel processing over surface modification is to create the inorganic oxide support in situ. Hence, without the limitation of the surface area of particles, more organic groups can be incorporated, even though their accessibility is not warranted. Another advantage is the possibility to... 

The interaction of Co2(CO)g and Co4(CO)i2 with many common inorganic supports as oxides and zeolites has been reported, and catalysts prepared from cobalt carbonyls have been used in the main reactions in which cobalt is used as active... 

In recent years, modification of zeolites, such as HZSM-5, by phosphoric compounds or metal oxides has been extensively studied, but little information is available on the modification of zeolites by diazomethane, which is an excellent methylating agent for protonic acidic sites. It is capable of entering into the small pores of zeolites because of its small molecular size and linear molecular structure. Yin and Peng (1,2) reported that the acidity and specific surface area of the inorganic oxide supports (AljOs, SiOj) and zeolite catalysts... 

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