Thymine dimerization in DNA model systems: Cyclobutane photolesion is predominantly formed via the singlet channel

Journal of the American Chemical Society

Volumn 131, Issue 14, 2009, Pages 5038-5039

  Schreier, Wolfgang J ^a,b,c   Kubon, Julia ^a,b,c   Regner, Nadja ^a,b,c   Haiser, Karin ^a,b,c   Schrader, Tobias E ^a,b,c   Zinth, Wolfgang ^a,b,c   Clivio, Pascale ^a,b   Gilch, Peter ^a,b,c  

^a Munich Center for Integrated Protein Science   (Germany)

^b UNIVERSITÉ DE REIMS CHAMPAGNE ARDENNE   (France)

^c UNIVERSITY OF MUNICH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOBUTANE; DNA MODEL; FEMTOSECOND IR SPECTROSCOPY;

BUTANE; DNA; NUCLEIC ACIDS; OLIGOMERS;

GENES;

DNA; PYRIMIDINE DIMER; THYMIDINE PHOSPHATE; THYMINE;

ARTICLE; CONFORMATIONAL TRANSITION; CONTROLLED STUDY; DIMERIZATION; DNA STRUCTURE; ILLUMINATION; IRRADIATION; LIGHT ABSORPTION; MOLECULAR MODEL; PHOTOREACTIVITY; QUANTUM YIELD; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; INFRARED SPECTROPHOTOMETRY; METABOLISM; TIME; ULTRAVIOLET RADIATION;

DNA; MODELS, MOLECULAR; NUCLEIC ACID CONFORMATION; PYRIMIDINE DIMERS; SPECTROPHOTOMETRY, INFRARED; THYMINE; TIME FACTORS; ULTRAVIOLET RAYS;

EID: 67749129320     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja900436t     Document Type: Article

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