Literature DB >> 26620786

Strong Two-Photon Circular Dichroism in Helicenes:  A Theoretical Investigation.

Branislav Jansík1,2,3,4, Antonio Rizzo1,2,3,4, Hans Ågren1,2,3,4, Benoit Champagne1,2,3,4.   

Abstract

Using a recently derived origin-invariant quadratic response approach combined with time-dependent density functional theory, four representative helicenes are shown to present a very strong two-photon circular dichroism (TPCD) response, which makes them candidates for the first experimental observation of a TPCD effect. The large response is attributed to the unique combination of chirality and electron delocalization. Comparison with electronic circular dichroism and two-photon absorption (TPA) shows that the three effects exhibit complementary features for unravelling the molecular structures. In particular, for the four (M)-helicenes studied here, the first, i.e., low-energy, dominant Cotton band is always negative, whereas for TPCD it is positive. From an analysis of the frontier orbitals describing most of the one-electron excitation vectors, the largest TPCD response of tetramethoxy-bisquinone-dithia-[7]-helicene has been attributed to the charge-transfer character of the excited state, like for the parent TPA effect. Moreover, the TPCD intensities are found to be mostly governed by the electric and magnetic dipole contributions, while the electric quadrupole terms are, on a relative basis, less important.

Entities:  

Year:  2008        PMID: 26620786     DOI: 10.1021/ct700329a

Source DB:  PubMed          Journal:  J Chem Theory Comput        ISSN: 1549-9618            Impact factor:   6.006


  3 in total

1.  Excitation and circular dichroism spectra of (+)-(S,S)-bis(2-methylbutyl)chalcogenides.

Authors:  Yasushi Honda; Atsushi Kurihara; Yusuke Kenmochi; Masahiko Hada
Journal:  Molecules       Date:  2010-03-31       Impact factor: 4.411

Review 2.  Two-photon polarization dependent spectroscopy in chirality: a novel experimental-theoretical approach to study optically active systems.

Authors:  Florencio E Hernández; Antonio Rizzo
Journal:  Molecules       Date:  2011-04-18       Impact factor: 4.411

3.  Alternating oligo(o,p-phenylenes) via ruthenium catalyzed diol-diene benzannulation: orthogonality to cross-coupling enables de novo nanographene and PAH construction.

Authors:  Zachary A Kasun; Hiroki Sato; Jing Nie; Yasuyuki Mori; Jon A Bender; Sean T Roberts; Michael J Krische
Journal:  Chem Sci       Date:  2018-08-30       Impact factor: 9.825

  3 in total

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