ch/pi hydrogen bonds in organic and organometallic chemistry pdf

Ch/pi Hydrogen Bonds In Organic And Organometallic Chemistry Pdf

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In proteins 11 of 20 natural amino acids and in DNA or RNA all four nucleic acids are involved in this type interaction. Five conclusion points are abstracted from the calculation results.

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Theoretical study on the polar hydrogen-π (Hp-π) interactions between protein side chains

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Focusing on the phenyl ring of Phe6 adjacent to the alkyl chain of Lys, the mutants for these amino acid residues were characterized. In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed.

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Theoretical study on the polar hydrogen-π (Hp-π) interactions between protein side chains

Thank you for visiting nature. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser or turn off compatibility mode in Internet Explorer. In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript. For the first time, the intermolecular orbital interaction between benzene and methane in the benzene-methane complex, a representative of weak interaction system, has been studied by us using ab initio calculations based on different methods and basis sets.

The Weak Hydrogen Bond: In Structural Chemistry and Biology

Organometallic compound , any member of a class of substances containing at least one metal -to- carbon bond in which the carbon is part of an organic group. Organometallic compounds constitute a very large group of substances that have played a major role in the development of the science of chemistry. They are used to a large extent as catalysts substances that increase the rate of reactions without themselves being consumed and as intermediates in the laboratory and in industry. The class includes such compounds as ferrocene , a remarkably stable compound in which an iron atom is sandwiched between two hydrocarbon rings.

Organometallic chemistry

Gautam Desiraju and Thomas Steiner

Quantum chemical calculations were used to investigate the Diels-Alder reactivities for a series of cycloalkenediones with tetrazine. We find that the reactivity trend of cycloalkenediones toward tetrazine is opposite to cycloalkenes. The electrostatic interactions between the cycloalkenediones and tetrazine become more stabilizing as the ring size of the cycloalkenediones increases, resulting in lower activation energies. The Diels-Alder reactivity trend of cycloalkenediones toward tetrazine is opposite that of cycloalkenes. The Diels-Alder reactivity trend of cycloalkenediones towards tetrazine is opposite of cycloalkenes. This is a preview of subscription content, access via your institution. Rent this article via DeepDyve.

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