Solid-state 17O NMR of thymine: a potential new probe to nucleic acid base pairing

2001 ◽  
pp. 891-892 ◽  
Author(s):  
Gang Wu ◽  
Shuan Dong ◽  
Ramsey Ida
2002 ◽  
Vol 59 (12) ◽  
pp. 792-799
Author(s):  
Takahiro HARADA ◽  
Takashi MIYAHARA ◽  
Naotoshi NAKASHIMA ◽  
Kazue KURIHARA

1991 ◽  
Vol 95 (4) ◽  
pp. 1530-1532 ◽  
Author(s):  
Anthony Harriman ◽  
Darren J. Magda ◽  
Jonathan L. Sessler

1999 ◽  
Vol 78 (1-2) ◽  
pp. 183-193 ◽  
Author(s):  
Ray Luo ◽  
Martha S. Head ◽  
James A. Given ◽  
Michael K. Gilson

2018 ◽  
Vol 114 (3) ◽  
pp. 89a
Author(s):  
Rongpeng Li ◽  
Chi H. Mak

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.


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