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The crystal structure of the 2:1 intermolecular complex containing 1-melhyl-5-flourouracil and 9-ethyl-2,6-diaminopurine

✍ Scribed by Ronald Chandross; Alexander Rich


Publisher
Wiley (John Wiley & Sons)
Year
1971
Tongue
English
Weight
640 KB
Volume
10
Category
Article
ISSN
0006-3525

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✦ Synopsis


RONAIdT) CHAXDROSS,* and -4TXXASDER RICH, Department o j Biology, lllassach usetts Itrstitute of Tochr/olo!i!j Camhrid~le, .Ilassachusettn 021.39

Synopsis

Two molerides of 1-methyl-.i-fiuorouracil complex with one molecule of 9-ethyl-2,-6diaminopririne and c*rystalliae in a triclinic unit cell. The crystal striwtiire w&q solved by analysis af 3dimensional x-ray diffraction data. A sharpened Patternon map was wed to determine the stnirtiire with a psiiedo-heavy atom technique. The three molecules form a planar hydrogen bonded net. One of the pyrimidines forms a triple hgdrogen bonded Watson-Crick pair with the purine, while the other pyrimidine forms hydrogen bonds to adenine through the imidaxole nitrogen. The network is completed by purine-purine hydrogen bonds.


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The crystal of the 1: 1 complex of ethyl laurate with heptakis(2,3,6-tri-0-methyl)cyclomaltoheptaose (ThI-@CD, permethyIated &cyclodextrin) is orthorombic, P&2,2,, with a = 14.796(Z), b m 22.444(6), c = 27.720@) A; V = 9~5(4) k3; and Z = 4. The macrocycles have a distorted ~nfo~ation due to the abse