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						<h1 itemprop="headline">Talk - Ksenia Bravaya: &quot;Electronic resonances in photoactive biomolecules&quot; Chem. Dep.</h1>
						
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									<p><strong>Location: </strong>Aud VI (Chemistry), Room 1510-213
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<p><strong>Title: </strong>"Electronic resonances in photoactive biomolecules"
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<p><strong>Speaker: </strong>Dr. Ksenia Bravaya,
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<p>Department of Chemistry, Boston University
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<p><strong>Web:</strong> <a href="http://people.bu.edu/kbravgrp/index.html" target="_blank" rel="noreferrer">http://people.bu.edu/kbravgrp/index.html</a>
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<p><br>&nbsp;<br><strong>Abstract:</strong><br>Photoinduced electron transfer lies in the basis of such processes as<br>photosynthesis, DNA damage repair by photolyases, and many others.<br>Bottom-up approach to understanding these complex processes implies,<br>first, understanding the photoinduced processes in the isolated<br>biochromophores. Commonly, excited electronic states of the<br>biochromophores exhibit metastable character with respect to electron<br>detachment (autoionizing resonances), and, thus, possess finite<br>lifetime. The information on the lifetime of the resonance is,<br>therefore, of primary importance for disentangling complex<br>photoinduced dynamics in the systems.<br><br>I will discuss the recent progress in the development of electronic<br>structure methods capable of description of resonance electronic<br>states.&nbsp; The methods are based on the equation-of-motion<br>coupled-cluster model with single and double substitutions (EOM-CCSD)<br>combined with complex-absorbing potential (CAP) technique [1]. The<br>performance of the method for description of autoionizing states in<br>medium-sized molecules of biological relevance will be demonstrated<br>[2].<br><br>[1] D. Zuev, T.C. Jagau, K.B. Bravaya, E. Epifanovsky, Y. Shao, E.<br>Sundstrom, M. Head-Gordon, and A.I. Krylov, J. Chem. Phys. 141 (2014)<br>024102.<br>[2] A.A. Kunitsa and K.B. Bravaya J. Phys. Chem. Lett. 6 (2015) 1053–1058.<br><br></p>
								
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