Ethylene glycol esters study

Pressure Dependence Studies. The variation of the product distribution as a function of total pressure for the optimum Ru/Rh/EtaN/HOAc system at 1000 atm and 230°C is illustrated in Figure 2. As found in much previous work this once again highlights the very strong pressure requirement for the formation of C2 products, particularly ethylene glycol esters. In contrast however, the rate of formation of methyl acetate is relatively independent of... 

Oligomeric PET model compounds have been widely used to study enzymatic hydrolysis of PET, since their degradation is faster and easier to analyze compared to a polymeric substrate. Diethyl terephthalate (DET), diethyl p-phthalate (DP), h/i(benzoyloxyethyl) terephthalate (PET trimer), ethylene glycol dibenzyl ester (BEB), and hA-(p-methylbenzoic acid)-ethylene glycol ester (PET dimer) have been employed (Eig. 2). Their degradation by PET hydrolases from Fusarium solani [27, 38], T. insolens [1, 5, 48, 101], P. mendocina [25, 49], T. fusca [26, 27, 38], Burkholderia cepacia [26, 27, 38], Aspergillus oryzae [103], Bacillus spp. [87], and porcine liver esterase [109, 110] has been reported, and the corresponding hydrolysis products have been partially characterized (Table 1). 

Studies by Bayer et aL [22] and Mutter [69] have shown that l uid-phase synthesis of peptides exhibits kinetic behaviour analogous to classic peptide synthesis. The reaction rates of both methods are trf the same order of magnitude, and using poly(ethylene glycol) esters, the polymer reaction proceeds at an even higher rate than the reaction involving the corresponding low-... 

In these studies cleavage of the endocyclic alkoxy group produces ethylene glycol and since only about 5% was found, it was concluded that hydrolysis proceeds 95% via exocyclic cleavage, in excellent agreement with results found for poly(ortho esters). 

Solutions of Ru3(CO)i2 in carboxylic acids are active catalysts for hydrogenation of carbon monoxide at low pressures (below 340 atm). Methanol is the major product (obtained as its ester), and smaller amounts of ethylene glycol diester are also formed. At 340 atm and 260°C a combined rate to these products of 8.3 x 10 3 turnovers s-1 was observed in acetic acid solvent. Similar rates to methanol are obtainable in other polar solvents, but ethylene glycol is not observed under these conditions except in the presence of carboxylic acids. Studies of this reaction, including infrared measurements under reaction conditions, were carried out to determine the nature of the catalyst and the mechanism of glycol formation. A reaction scheme is proposed in which the function of the carboxylic acid is to assist in converting a coordinated formaldehyde intermediate into a glycol precursor. 

The reaction of the p-nitrophenyl esters with the polymer (4) was studied in dimethyl sulfoxide ( DMSO ) solution in the presence of triethylamine at 25°C. The poly-L-lysine derivatives obtained have different IR absorption spectra from those of the starting compounds, and have absorptions assigned to the nucleic acid bases. Poly( e,N-Ade-L-lysine )(5) was soluble in DMSO and ethylene glycol, and also in water below pH 3, where it was present as a protonated form. In dimethylformamide (... 

In order to study the effect of substituents near the hydrolyzable bond, four fatty acid ethoxylates with different degrees of steric hindrance near the ester bond, see Fig. 4, have been synthesized [18]. The homologue pure surfactants were prepared by reacting the appropriate acid chlorides with a large excess of tetra(ethylene glycol) in the presence of pyridine. 

Fermentation-derived organic acids and their esters are potentially important chemical feedstocks for polymers and specialty polymers, but most significantly as alternative solvents for industrial and consumer applications. For example, lactate esters are derived from renewable carbohydrate raw materials such as cornstarch. They exhibit much lower toxicity compared with halogenated hydrocarbons and ethylene glycol ethers and are environmentally benign. Some studies suggested that lactate ester solvents have the potential of replacing petroleum-based solvents... 

As far as quantitative chemical derivatization GC analysis is concerned, it is necessary to mention especially the work of Gehrke and his collaborators, who specified the fundamental concepts of quantitative GC analysis combined with the chemical derivatization of sample compounds and applied them to the accurate determination of the twenty natural protein amino acids and other non-protein amino acids as their N-TFA-n-butyl esters [5 ], the urinary excretion level of methylated nucleic acid bases as their TMS derivatives [6], TMS nucleosides [7] and other investigations. Further examples include a computer program for processing the quantitative GC data obtained for seventeen triglyceride fatty acids after their transesterification by 2 NKOH in n-butanol [8], a study of the kinetics of the transesterification reactions of dimethyl terephthalate with ethylene glycol [9] and the GC-MS determination of chlorophenols in spent bleach liquors after isolation of the chlorophenols by a multi-step extraction, purification of the final extract by HPLC and derivatization with diazoethane [10]. 

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