Core-modified meso-aryl hexaphyrins with an internal thiophene bridge: structure, aromaticity, and photodynamics.
about
5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents.Macrocyclic bis(phenanthroline-pyrrole): a convenient one-pot synthesis, structure(s), spectroscopic, and redox properties, and the binding of amine guests, protons, and lanthanide ions.Conformational change from a twisted figure-eight to an open-extended structure in doubly fused 36π core-modified octaphyrins triggered by protonation: implication on photodynamics and aromaticity.Bicyclic Baird-type aromaticity.Internally 2,5-Thienylene-Bridged [46]Decaphyrin: (Annuleno)annulene Network Consisting of Möbius Aromatic Thia[28]hexaphyrins and Strong Hückel Aromaticity of its Protonated Form.Aromaticity switching via azulene transformations in azulene-bridged A,D-dithiahexaphyrin.Thiophene-fused dithiaoctaphyrins: π-system switching between cross-conjugated and macrocyclic π-networks.Modulation of dual electronic circuits of [26]hexaphyrins using internal aromatic straps.
P2860
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P2860
Core-modified meso-aryl hexaphyrins with an internal thiophene bridge: structure, aromaticity, and photodynamics.
description
2013 nî lūn-bûn
@nan
2013年の論文
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2013年学术文章
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2013年学术文章
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2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Core-modified meso-aryl hexaph ...... romaticity, and photodynamics.
@en
Core-modified meso-aryl hexaph ...... romaticity, and photodynamics.
@nl
type
label
Core-modified meso-aryl hexaph ...... romaticity, and photodynamics.
@en
Core-modified meso-aryl hexaph ...... romaticity, and photodynamics.
@nl
prefLabel
Core-modified meso-aryl hexaph ...... romaticity, and photodynamics.
@en
Core-modified meso-aryl hexaph ...... romaticity, and photodynamics.
@nl
P2093
P2860
P356
P1476
Core-modified meso-aryl hexaph ...... romaticity, and photodynamics.
@en
P2093
A Srinivasan
Ganesan Karthik
Jong Min Lim
Mahima Sneha
Tavarekere K Chandrashekar
V Prabhu Raja
P2860
P304
P356
10.1002/CHEM.201203737
P407
P50
P577
2013-01-04T00:00:00Z