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Biocomplementary interaction behavior in DNA‐like and RNA‐like polymers
Author(s) -
Cheng ChihChia,
Yen YingChieh,
Ye YunSheng,
Chang FengChih
Publication year - 2009
Publication title -
journal of polymer science part a: polymer chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.768
H-Index - 152
eISSN - 1099-0518
pISSN - 0887-624X
DOI - 10.1002/pola.23679
Subject(s) - atom transfer radical polymerization , thymine , nucleobase , chemistry , hydrogen bond , polymer chemistry , supramolecular chemistry , base pair , polymer , dna , copolymer , differential scanning calorimetry , titration , uracil , polymerization , crystallography , stereochemistry , molecule , organic chemistry , crystal structure , biochemistry , physics , thermodynamics
A series of nucleobased polymers and copolymers were synthesized through atom transfer radical polymerization (ATRP). Biocomplementary DNA‐ and RNA‐like supramolecular complexes are formed in dilute DMSO solution through nucleobase recognition. 1 H NMR titration studies of these complexes in CDCl 3 indicated that thymine‐adenine (T‐A) and uracil‐adenine (U‐A) complexes form rapidly on the NMR time scale with high association constants (up to 534 and 671 M –1 , respectively) and result in significant T g increase. WAXD and differential scanning calorimetry analyzes in the bulk state indicate the presence of highly physical cross‐linked structures and provide further details into the nature of the self‐assembly of these systems. Furthermore, this study is of discussion on the difference in the hydrogen bond strength between T‐A and U‐A base pairs within polymer systems, indicating that the strength of hydrogen bonds in RNA U‐A pairs is stronger than that in DNA T‐A base pairs. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 6388–6395, 2009

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