Thermal elimination during synthesis

Niobium and titanium incorporation in a molecular sieve can be achieved either by hydrothermal synthesis (direct synthesis) or by post-synthesis modification (secondary synthesis). The grafting method has shown promise for developing active oxidation catalyst in a simple and convenient way. Recently, the grafting of metallocene complexes onto mesoporous silica has been reported as alternate route to the synthesis of an active epoxidation catalyst [21]. Further the control of active sites, the specific removal of organic material (template or surfactant) occluded within mesoporous molecular sieves during synthesis can also be important and useful to develop an active epoxidation catalyst. Thermal method is quite often used to eliminate organic species from porous materials. However, several techniques such as supercritical fluid extraction (SFE) and plasma [22], ozone treatment [23], ion exchange [24-26] are also reported. 

The preparation of poly(2,5 dimethoxy phenylene vinylene)(DM-PPV) utilized the xanthate precursor route. Many similarities exist between the PPV xanthate thermal elimination and this PPV derivative. Previous studies had attempted to synthesis DM-PPV using the SPR method. The SPR resulted in gel formation during dialysis so that film casting was not possible. The XPR was successful in preparing precursor films that can be thermally converted to DM-PPV. The derivatives of PPV are useful to prepare a polymer with a shift in the absorbance and photoluminescence maximum. DM-PPV exhibits an 100 nm red shift as compared with PPV synthesized via the XPR. 

In situ infrared spectroscopy (heated cell) and TGA-IR (evolved gas product analysis) are important tools that have been used to characterize the thermal elimination reaction in the synthesis of PPV and PPV derivatives using the precursor route. A detailed understanding of the reaction is important as the conditions of the reaction influence the properties of the resultant polymer product. The mechanism of the thermal elimination reaction can be characterized using in situ spectroscopy. Both an El and an E2 mechanism appears to be operating during the thermal conversion of PPV... 

It is important to note that the by-products are minimized during DMSS synthesis and/or eliminated during the separation stage. Any persisting residues then will be eliminated during the subsequent stages of quinacridone production (thermal or PPA) ensuring no contribution to impurity formation in the final products. 

Ketene acetal synthesis by /1-elimination of haloacids from halogenated acetals under well controlled conditions using thermal activation (A), ultrasound (US) or micro-wave irradiation [92] (MW) has been described. From a mechanistic point of view, as the TS is more charge delocalized than the GS and the polarity is enhanced during the course of the reaction, a favorable microwave effect can therefore be observed (Eqs. (37) and (38) and Scheme 3.13). 

S -Methylxanthates 62 derived from the same alcohols 50 are thermally less stable than the corresponding carbamates 57. They decompose during their synthesis according to two competitive elimination pathways, ft C—H and ft C—Si (3/2) eliminations14 (Scheme 12), giving rise to a lower metallole yield than from carbamates 57. 

Depolymerization is a special case of thermal degradation. It can be observed particularly in polymers based on a, a -disubstituted monomers. In these, degradation is a reversal of the synthesis process. It is a chain reaction during which the monomers are regenerated by an unzipping mechanism. This is due to the low polymerization enthalpy of these polymers. For the thermal fission of polymers with secondary and tertiary C-atoms, higher energies are required. In these cases elimination reactions occur. This can be seen very clearly in PVC and PVAC. 

Elimination of the yellowing introduced by the stable nitroxyl radicals was essential for commercial development of these excellent stabilizers. Since phenolic antioxidants are necessary for the thermal stabilization of polymers during processing, we turned our attention to ways in which unfavorable interactions between the hindered phenols and the stabilizing nitroxyl radicals could be avoided. In this section we describe the discovery of the light-stabilizing activity of hindered amine compounds, an improved synthetic method for these compounds, the synthesis of a number of derivatives, and the evaluation of their stabilizing activity. 

During the past few years, Weinreb and co-workers have published a series of papers on studies of intramolecular imino Diels-Alder cycloadditions and applications of this methodology to alkaloid total synthesis.84 These cycloadditions have involved Af-acylimines as the dienophiles, generated thermally (hot tube pyrolysis) by acetic acid elimination of methy-lol acetates [Eq. (26)].85... 

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