نتایج جستجو برای: amide iminol tautomerism

تعداد نتایج: 14426  

Journal: :Acta Crystallographica Section E Structure Reports Online 2012

Journal: :Dalton transactions 2014
Bernhard Breit Urs Gellrich Timothy Li Jason M Lynam Lucy M Milner Natalie E Pridmore John M Slattery Adrian C Whitwood

A combined computational and experimental study is presented that investigates the mechanism of the anti-Markovnikov hydration of phenylacetylene by [Ru(η(5)-C5H5)(6-DPPAP)(3-DPICon)](+) (where 6-DPPAP = 6-(diphenylphosphino)-N-pivaloyl-2-aminopyridine) and 3-DPICon = 3-diphenylphosphinoisoquinolone). The proposed mechanism, modelled using density functional calculations, involves an initial al...

2003
Wojciech P. Ozimiński Jan Cz. Dobrowolski Aleksander P. Mazurek

DFT (B3PW91/6-311þþG**), ab initio (HF/6-311þþG**), and single point CCSD(T)/6-311þþG**//B3PW91/6311þþG** calculations were performed to investigate the stability and tautomerism of the C5-substituted 1,2,3-triazoles. Three different tautomers are possible for the substituted 1,2,3-triazoles: N1–H, N2–H, and N3–H. For all the substituents applied, the most stable is the N2–H tautomer. Out of th...

Journal: :Journal of the American Chemical Society 2005
Hubert Piwoński Clemens Stupperich Achim Hartschuh Jerzy Sepioł Alfred Meixner Jacek Waluk

Fluorescence imaging is used to visualize directly the transfer of two inner hydrogen atoms in single porphycene molecules. This reaction leads to a chemically equivalent but differently oriented structure and hence results in a rotation of the transition dipole moments. By probing single immobilized molecules with an azimuthally polarized laser beam in the focal spot of a confocal microscope w...

Journal: :journal of the iranian chemical research 0
ewa daniela raczyńska department of chemistry, warsaw university of life sciences, 02-776 warszawa, poland malgorzta hallmann department of chemistry, warsaw university of life sciences, 02-776 warszawa, poland kinga duczmal department of chemistry, warsaw university of life sciences, 02-776 warszawa, poland

keto-enol tautomerism was investigated for ionized pyruvic acid using the dft(b3lyp) method and the larger basis sets [6-31++g(d,p), 6-311++g(3df, 3pd) and aug-cc-pvdz]. change of the tautomeric preference was observed when going from the neutral to ionized tautomeric mixture. ionization favors the enolization process (ketoenol) of pyruvic acid, whereas the ketonization (ketoenol) is preferred ...

Journal: :Journal of the American Chemical Society 2005

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