Indandiazocines: Unidirectional molecular switches

We report theoretical investigations on azobenzene-based indandiazocines, novel chiral systems that perform unidirectional cis↔trans isomerizations upon photo-excitation. For three different systems of this kind, we have simulated excited-state surface-hopping trajectories for both isomerization...

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Main Authors: Bernd Hartke, Tim Raeker
Format: Article
Language:English
Published: ScienceOpen 2015-01-01
Series:ScienceOpen Research
Online Access:https://www.scienceopen.com/document?vid=bdd94554-c0d3-4aeb-87f7-73b1bf98d860
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spelling doaj-5c6c6ff425cb4c5eadbd3207873d4a422020-12-15T17:21:32ZengScienceOpenScienceOpen Research2199-10062015-01-0110.14293/S2199-1006.1.SOR-CHEM.ARDTLN.v1Indandiazocines: Unidirectional molecular switchesBernd HartkeTim RaekerWe report theoretical investigations on azobenzene-based indandiazocines, novel chiral systems that perform unidirectional cis↔trans isomerizations upon photo-excitation. For three different systems of this kind, we have simulated excited-state surface-hopping trajectories for both isomerization directions, using a configuration-interaction treatment based on system-specifically reparametrized semiempirical AM1 theory. Our results are also compared to experimental and theoretical results for the parent system diazocine. We show that, as intended by design, the trans→cis bending of the azo unit in these indandiazocines can only happen in one of the two possible directions due to sterical constraints, which is a new feature for photoswitches and a necessary prerequisite for directional action at the nanoscale.https://www.scienceopen.com/document?vid=bdd94554-c0d3-4aeb-87f7-73b1bf98d860
collection DOAJ
language English
format Article
sources DOAJ
author Bernd Hartke
Tim Raeker
spellingShingle Bernd Hartke
Tim Raeker
Indandiazocines: Unidirectional molecular switches
ScienceOpen Research
author_facet Bernd Hartke
Tim Raeker
author_sort Bernd Hartke
title Indandiazocines: Unidirectional molecular switches
title_short Indandiazocines: Unidirectional molecular switches
title_full Indandiazocines: Unidirectional molecular switches
title_fullStr Indandiazocines: Unidirectional molecular switches
title_full_unstemmed Indandiazocines: Unidirectional molecular switches
title_sort indandiazocines: unidirectional molecular switches
publisher ScienceOpen
series ScienceOpen Research
issn 2199-1006
publishDate 2015-01-01
description We report theoretical investigations on azobenzene-based indandiazocines, novel chiral systems that perform unidirectional cis↔trans isomerizations upon photo-excitation. For three different systems of this kind, we have simulated excited-state surface-hopping trajectories for both isomerization directions, using a configuration-interaction treatment based on system-specifically reparametrized semiempirical AM1 theory. Our results are also compared to experimental and theoretical results for the parent system diazocine. We show that, as intended by design, the trans→cis bending of the azo unit in these indandiazocines can only happen in one of the two possible directions due to sterical constraints, which is a new feature for photoswitches and a necessary prerequisite for directional action at the nanoscale.
url https://www.scienceopen.com/document?vid=bdd94554-c0d3-4aeb-87f7-73b1bf98d860
work_keys_str_mv AT berndhartke indandiazocinesunidirectionalmolecularswitches
AT timraeker indandiazocinesunidirectionalmolecularswitches
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