Toward helical-shaped diradicaloids: cyclobutenyl o-quinodimethane-bridged indeno[1,2-b]fluorenes

Open-shell diradicaloids have been intensively investigated recently due to their attractive and unique optical, electronic and magnetic properties. However, open-shell diradicaloids with non-planar conjugated frameworks are less studied, especially helical-shaped pi systems. In this work, we synthe...

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Veröffentlicht in:Chemical communications (Cambridge, England) Jg. 54; H. 81; S. 11383 - 11386
Hauptverfasser: Qiu, Shuhai, Wang, Chaoqiang, Xie, Sheng, Huang, Xiaobo, Chen, Lanlan, Zhao, Yunhui, Zeng, Zebing
Format: Journal Article
Sprache:Englisch
Veröffentlicht: CAMBRIDGE Royal Soc Chemistry 09.10.2018
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ISSN:1359-7345, 1364-548X
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Abstract Open-shell diradicaloids have been intensively investigated recently due to their attractive and unique optical, electronic and magnetic properties. However, open-shell diradicaloids with non-planar conjugated frameworks are less studied, especially helical-shaped pi systems. In this work, we synthesized tetraindeno-based singlet biradicals in a helical geometry, bridged by a curved cyclobutenyl o-quinodimethane molecule. Large diradical characters and extremely small singlet-triplet energy gaps, as well as unusual half-field transitions (forbidden Delta M-s = 2) were revealed for these 3D diradicals.
AbstractList Open-shell diradicaloids have been intensively investigated recently due to their attractive and unique optical, electronic and magnetic properties. However, open-shell diradicaloids with non-planar conjugated frameworks are less studied, especially helical-shaped π systems. In this work, we synthesized tetraindeno-based singlet biradicals in a helical geometry, bridged by a curved cyclobutenyl o-quinodimethane molecule. Large diradical characters and extremely small singlet-triplet energy gaps, as well as unusual half-field transitions (forbidden ΔMs = 2) were revealed for these 3D diradicals.
Open-shell diradicaloids have been intensively investigated recently due to their attractive and unique optical, electronic and magnetic properties. However, open-shell diradicaloids with non-planar conjugated frameworks are less studied, especially helical-shaped pi systems. In this work, we synthesized tetraindeno-based singlet biradicals in a helical geometry, bridged by a curved cyclobutenyl o-quinodimethane molecule. Large diradical characters and extremely small singlet-triplet energy gaps, as well as unusual half-field transitions (forbidden Delta M-s = 2) were revealed for these 3D diradicals.
Author Qiu, Shuhai
Zhao, Yunhui
Zeng, Zebing
Xie, Sheng
Wang, Chaoqiang
Huang, Xiaobo
Chen, Lanlan
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  organization: Hunan Univ, State Key Lab Chemo Biosensing & Chemometr, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China
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Issue 81
Keywords GROUND-STATE
CORANNULENE
RADICALS
CLOSED-SHELL
HYDROCARBON
EXTENDED P-QUINODIMETHANES
MOLECULES
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Snippet Open-shell diradicaloids have been intensively investigated recently due to their attractive and unique optical, electronic and magnetic properties. However,...
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Chemistry, Multidisciplinary
Physical Sciences
Science & Technology
Title Toward helical-shaped diradicaloids: cyclobutenyl o-quinodimethane-bridged indeno[1,2-b]fluorenes
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