Search results for " Alcohol."
showing 10 items of 568 documents
Answer to the Letter to the Editor by Dr. Sanjay Pralhad Shirsat concerning the article “Separation of isobutyl alcohol and isobutyl acetate by extra…
2015
1981
In order to investigate the influences of different end-groups on oligomer miscibility with other substances, oligo(propylene glycol)s bearing OH groups (OPG-OH) studied in the previous paper2, were acetylated at both ends (OPG-AC). The limits of miscibility of OPG-AC with oligo(dimethylsiloxane) (ODMS) were measured turbidimetrically. A simple and reliable method for the determination of the critical points from turbidity data is presented. The observed upper critical temperatures (Tc) increase with degree of oligomerization of ODMS (ranging from 1 to 5), whereas Tc shows a minimum when the degree of oligomerization of the OPG-AC is raised (from 1 to 57,5). For lower mol. wt. oligoglycols,…
Micellar fluorescence enhancement of carbamate pesticides
1990
Abstract Different studies have been carried out on the interaction of carbamate pesticides, such as carbofuran and carbaryl, with nonionic and anionic surfactants. Micellar fluorescence enhancements (MEF) of 15–20 for carbofuran in the presence of fatty alcohol ethylene oxide condensates, and of 3.7–8.6 in the presence of anionic surfactants at neutral pH have been obtained. Carbaryl does not interact with surfactants, but when it is hydrolysed to 1-naphthol, MEF values of the order of 2 are obtained in the presence of nonylphenol ethylene oxide condensates. The experimental parameters have been optimized in order to obtain maximum fluorescence. The mechanisms involved in the fluorescence …
STUDIEN ZUM VORGANG DER WASSERSTOFFÜBERTRAGUNG 611
1982
Abstract In arylsulfonyl halides, the half-wave potentials of the corresponding chlorides and fluorides differ by more than 1000 mV, the fluoride being more negative; the influence of para-substituents is small for the chlorides, large for the fluorides. In agreement with the half-wave potentials, arylsulfonyl chlorides are considerably more reactive chemically than the corresponding fluorides. The O-selectivity found for P(O)F compounds is not observed in arylsulfonyl fluorides. Studies of competitive ester formation using primary and secondary alcohols and various arylsulfonyl chlorides yielded no clear analogy to the half-wave potentials. The primary alcohol is always sulfonated in prefe…
Polyfurfuryl alcohol composite as adsorbent of polychlorinated biphenyls and pyrethroid insecticides
2007
Abstract Composites from furfuryl alcohol and silica gel were prepared in dichloromethane using trifluoroacetic acid as catalyst and characterized by means of thermogravimetric analysis, transmission electron microscopy and nitrogen adsorption–desorption isotherms. The polymer content in the composites ranged between 19.5% and 32.9%. The capability to adsorb polychlorinated biphenyls and pyrethroid insecticides was tested for composite samples containing different percentages of polymer. Pyrethroids are retained almost totally by composites containing around 24–33% of polymer, while recovery of PCBs close to 80% is obtained with all the composites. No selectivity between compounds of the sa…
Evaluación de Consecuencias derivadas del Consumo de Alcohol (ECCA)
2019
Escala de evaluación de consecuencias derivadas derivadas del consumo de alcohol
1,1-Diphenyl-4-(thiophen-2-yl)but-3-yn-1-ol
2018
The asymmetric unit of the title homopropargyl alcohol, C20H16OS, contains two independent molecules comprising a hydroxy group, a 3-(2-thiophenyl)- propargylic moiety and two aromatic rings linked to a central carbon atom. The two unique molecules are linked into a dimer by an O—HO hydrogen bond. In one molecule, the thiophene ring is disordered over two orientations rotated by 180 with a refined occupancy ratio of 0.575 (4):0.425 (4). The crystal structure is stabilized by O—H and C—H hydrogen-bond interactions. The crystal studied was a two-component non-merohedral twin, the refined ratio of the twin components being 0.575 (4):0.425 (4). UCR::Vicerrectoría de Docencia::Ciencias Básicas::…
Relationship between dysfunctional eating patterns and binge drinking in young people and associated risk factors
2022
La joventut (compresa entre els 18 i 30 anys) es considera un període de vulnerabilitat, en què és freqüent observar trastorns alimentaris, consum de drogues i una major tendència a buscar noves sensacions i comportaments de risc, entre moltes altres conductes. En concret, hi ha dos comportaments molt prevalents en els joves i s'associen amb conseqüències de salut molt negatives: el consum de menjar ultraprocessat i el consum d'alcohol. Tot i això, el problema no rau només en el tipus de consum (és a dir, beure alcohol o menjar menjar ràpid), sinó també en com es consumeix l'alcohol o el menjar. L'afartament es caracteritza per la ingesta de grans quantitats de menjar (afartament de menjar)…
Recent developments and applications of the chiral Brønsted acid catalyzed allylboration of carbonyl compounds
2018
The 50-year-old allylboration reaction has seen dramatic developments since the dawn of the new century after the first catalytic asymmetric versions came into play. In the past decade alone, several methodologies capable of achieving the desired homoallylic alcohols in over 90% ee have been developed. This review focuses on the chiral Brønsted acid catalyzed allylboration reaction, covering everything from the very first examples and precedents to modern day variations and applications.1 Introduction2 Early Developments3 Synthetic Applications4 Variants5 Computational Contribution6 Conclusions
Lipase-catalysed preparation of acyl derivatives of the germacranolide sesquiterpenoid cnicin
2009
Several acyl derivatives of cnicin were obtained through lipase-catalysed acylation and alcoholysis reactions. In most reactions lipases showed a regioselective behaviour affording only one product. Longer chain acyl derivatives were prepared at lower temperature than the used in lipase-catalysed reactions, to preclude side products formation. The enzymatic approach let to prepare a family of novel acetyl and fatty acid derivatives of cnicin which are not obtainable following traditional organic synthetic procedures.