C?H ? O hydrogen bonding in solutions of methylated nucleic acid base analogs as revealed by nmr

Biopolymers ◽  
1989 ◽  
Vol 28 (2) ◽  
pp. 589-604 ◽  
Author(s):  
V. I. Bruskov ◽  
V. N. Bushuev ◽  
M. S. Okon ◽  
N. V. Shulyupina ◽  
V. I. Poltev

2000 ◽  
Vol 145 (1) ◽  
pp. 142-146 ◽  
Author(s):  
Jiřı́ Czernek ◽  
Radovan Fiala ◽  
Vladimı́r Sklenář


2007 ◽  
Vol 17 (2) ◽  
pp. 246-252 ◽  
Author(s):  
Z. Q. Cao ◽  
W. G. Liu ◽  
D. C. Liang ◽  
G. Guo ◽  
J. Y. Zhang


2001 ◽  
Vol 114 (12) ◽  
pp. 5149-5155 ◽  
Author(s):  
Marcus Elstner ◽  
Pavel Hobza ◽  
Thomas Frauenheim ◽  
Sándor Suhai ◽  
Efthimios Kaxiras


2010 ◽  
Vol 63 (4) ◽  
pp. 631 ◽  
Author(s):  
Priscilla Johnston ◽  
Milton T.W. Hearn ◽  
Kei Saito

Procedures derived from bioinspired mechanisms are increasingly being used to create novel materials based on the principles of green chemistry. Thymine, a nucleic acid base in DNA, has the propensity to both hydrogen bond and photodimerize. Photodimerization of thymine occurs when irradiated at wavelengths of >270 nm and can be reversed by irradiation at wavelengths of <250 nm. In this investigation, n-alkyl-linked bis-thymines have been supramolecularly aligned with poly(vinyl pyrrolidone) templates by non-covalent hydrogen bonding, and photopolymerized in the solid state. Photo-depolymerization of the products was performed to complete the reversible polymerization.



1996 ◽  
Vol 14 (1) ◽  
pp. 6-11 ◽  
Author(s):  
H.A. Gabb ◽  
S.R. Sanghani ◽  
C.H. Robert ◽  
C. Prévost






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