Literature DB >> 14293226

HYDROGEN-BONDED DIMERS OF ADENINE AND URACIL DERIVATIVES.

R M HAMLIN, R C LORD, A RICH.   

Abstract

In concentrated solutions of either 9-ethyladenine or 1-cyclohexyluracil in deuterochloroform, absorption bands in the infrared spectrum demonstrate hydrogen bonding of the adenine and uracil derivatives with themselves. In dilute solutions, there is very little hydrogen bonding. However, when dilute solutions of 9-ethyladenine and 1-cyclohexyluracil are mixed, a series of bands appear which show that these molecules are hydrogen-bonding with each other much more strongly than with themselves. A study of the stoichiometry of this association indicates formation of 1:1 hydrogen-bonded pairs in solution.

Entities:  

Keywords:  ADENINE; CHEMISTRY; EXPERIMENTAL LAB STUDY; SPECTRUM ANALYSIS; URACIL

Mesh:

Substances:

Year:  1965        PMID: 14293226     DOI: 10.1126/science.148.3678.1734

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  10 in total

1.  The effect of substituents on the hydrogen bonding of adenine and uracil derivatives.

Authors:  Y Kyogoku; R C Lord; A Rich
Journal:  Proc Natl Acad Sci U S A       Date:  1967-02       Impact factor: 11.205

2.  The structure of a crystalline complex containing one phenobarbital molecule and two adenine derivatives.

Authors:  S H Kim; A Rich
Journal:  Proc Natl Acad Sci U S A       Date:  1968-06       Impact factor: 11.205

3.  A proton magnetic resonance study of the interaction of adenosine with polyuridylic Acid: evidence for both adenine-uracil base-stacking and base-pairing.

Authors:  B W Bangerter; S I Chan
Journal:  Proc Natl Acad Sci U S A       Date:  1968-08       Impact factor: 11.205

4.  Simulation protocols for coherent femtosecond vibrational spectra of peptides.

Authors:  Wei Zhuang; Darius Abramavicius; Tomoyuki Hayashi; Shaul Mukamel
Journal:  J Phys Chem B       Date:  2006-02-23       Impact factor: 2.991

5.  N-H stretching excitations in adenosine-thymidine base pairs in solution: pair geometries, infrared line shapes, and ultrafast vibrational dynamics.

Authors:  Christian Greve; Nicholas K Preketes; Henk Fidder; Rene Costard; Benjamin Koeppe; Ismael A Heisler; Shaul Mukamel; Friedrich Temps; Erik T J Nibbering; Thomas Elsaesser
Journal:  J Phys Chem A       Date:  2013-01-07       Impact factor: 2.781

6.  Van der Waals-London interactions and the configuration of hydrogen-bonded purine and pyrimidine pairs.

Authors:  B Pullman; P Claverie; J Caillet
Journal:  Proc Natl Acad Sci U S A       Date:  1966-04       Impact factor: 11.205

7.  Base-pairing configurations between purines and pyrimidines in the solid state: a 2:1 crystalline complex containing 1-methyl-5-iodouracil and 9-ethyl-2,6-diaminopurine.

Authors:  L L Labana; H M Sobell
Journal:  Proc Natl Acad Sci U S A       Date:  1967-02       Impact factor: 11.205

8.  Association by hydrogen bonding of mononucleotides in aqueous solution.

Authors:  M Raszka; N O Kaplan
Journal:  Proc Natl Acad Sci U S A       Date:  1972-08       Impact factor: 11.205

9.  The crystal and molecular structure of an intermolecular complex between riboflavin and an adenosine derivative.

Authors:  D Voet; A Rich
Journal:  Proc Natl Acad Sci U S A       Date:  1971-06       Impact factor: 11.205

10.  Crystal structure of a complex between lumiflavin and 2,6-diamino-9-ethylpurine: a flavin adenine dinucleotide model exhibiting charge-transfer interactions.

Authors:  F E Scarbrough; H Shieh; D Voet
Journal:  Proc Natl Acad Sci U S A       Date:  1976-11       Impact factor: 11.205

  10 in total

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