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Cooperative hydrogen bonding in solution: Influence of molecule structureInfluence of cooperative interactions on IR stretching vibration frequencies of complexes CCl3H

Stereochemistry of Seven-membered Heterocycles. XXXVI. Unprecedented Solvent Effect on Thermodynamical Parameters of Conformational Equilibrium of Model 1,2,3-Trithia-5,6-benzocycloheptene: Donor-Acceptor Interactions of Conformers with the Medium led us to conclusion that the observed effect depends on the donor-acceptor interaction of two

Hyperbranched polyester poly[3-(morpholin-4-yl)propionates] and their copper(II) complexes to IR and electronic spectroscopy data, each coordination entity in the complexes is an isolated

Polymorphism of Merocyanine Dyes Homologues with 1,3-Diethyl-2-thiobarbituric Acid Acceptor and p-Dimethylaminobenzene Donor and Different Polymethine Chains Connecting Them and p-dimethylaminobenzene with different lengths of the polymethine bridge between donor and acceptor

Protic Ionic Liquid as Reagent, Catalyst, and Solvent: 1-Methylimidazolium Thiocyanate ionic liquids for the ring-opening of donor-acceptor cyclopropanes. A wide variety of activated

4-(Dimethylamino)Pyridinium Azide in Protic Ionic Liquid Media as a Stable Equivalent of Hydrazoic Acid hydrazoic acid. The synthetic utility of this system was demonstrated using donor-acceptor cyclopropane ring

Effect of cation structure on the formation of hydrogen bond between ionic liquids and solute molecules acceptor ability of ionic liquids from the Kamlet-Abboud-Taft equation and the proton donor ability

A new method for the extraction of specific interaction enthalpy from the enthalpy of solvation' or homomorph are not required. This method is applicable not only for proton-donor solutes but also

Expanding the Reactivity of Donor-Acceptor Cyclopropanes: Synthesis of Benzannulated Five-Membered Heterocycles via Intramolecular Attack of a Pendant Nucleophilic GroupLewis-acid-induced domino transformations of donor-acceptor cyclopropanes, possessing a

A new method for the extraction of specific interaction enthalpy from the enthalpy of solvation' or homomorph are not required. This method is applicable not only for proton-donor solutes but also

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