J 2013

Photochemistry of 2-Aminooxazole, a Hypothetical Prebiotic Precursor of RNA Nucleotides

SZABLA, Rafal Kazimierz, Deniz TUNA, Robert W GORA, Jiří ŠPONER, Andrzej L SOBOLEWSKI et. al.

Basic information

Original name

Photochemistry of 2-Aminooxazole, a Hypothetical Prebiotic Precursor of RNA Nucleotides

Authors

SZABLA, Rafal Kazimierz (616 Poland), Deniz TUNA (276 Germany), Robert W GORA (616 Poland), Jiří ŠPONER (203 Czech Republic, guarantor, belonging to the institution), Andrzej L SOBOLEWSKI (616 Poland) and Wolfgang DOMCKE (276 Germany)

Edition

Journal of Physical Chemistry Letters, Washington, American Chemical Society, 2013, 1948-7185

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

10403 Physical chemistry

Country of publisher

United States of America

Confidentiality degree

není předmětem státního či obchodního tajemství

References:

Impact factor

Impact factor: 6.687

RIV identification code

RIV/00216224:14740/13:00069531

Organization unit

Central European Institute of Technology

UT WoS

000323300900032

Keywords in English

EXCITED-STATE DYNAMICS; REPULSIVE (1)PI-SIGMA-ASTERISK STATES; CONICAL INTERSECTIONS; BUILDING-BLOCKS; AB-INITIO; PYRROLE; MOLECULES; SYSTEMS; PHOTOPHYSICS; DRIVEN

Tags

Tags

International impact, Reviewed
Změněno: 1/10/2013 09:57, Olga Křížová

Abstract

V originále

2-Aminooxazole has recently been proposed as a hypothetical precursor of RNA nucleotides on early earth. UV irradiation was considered as a crucial environmental factor in the proposed reaction sequence. We report on state-of-the-art multireference quantum-chemical calculations elucidating the possible nonradiative deactivation channels of this compound. According to our findings, the gas-phase photochemistry of 2-aminooxazole should be dominated by the photodetachment of the hydrogen atom of the NH2 group via a (1)pi sigma(NH)* state leading either to ultrafast nonradiative deactivation, phototautomerization, or photodissociation of a hydrogen atom. We also identified a possible ring-opening reaction and a ring-puckering process that could occur after electronic excitation. These reactions seem to be less probable because they are driven by a higher-lying excited singlet state and are inherently slower than the hydrogen-atom dynamics.

Links

ED1.1.00/02.0068, research and development project
Name: CEITEC - central european institute of technology