The excited state antiaromatic benzene ring: a molecular Mr Hyde? - Wikidata - awgldk - TriplyDB

The excited state antiaromatic benzene ring: a molecular Mr Hyde?

The excited state antiaromatic benzene ring: a molecular Mr Hyde?

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Metal-free photochemical silylations and transfer hydrogenations of benzenoid hydrocarbons and graphene Analysis of a Compound Class with Triplet States Stabilized by Potentially Baird Aromatic [10]Annulenyl Dicationic Rings.A Computational Investigation of the Substituent Effects on Geometric, Electronic, and Optical Properties of Siloles and 1,4-Disilacyclohexa-2,5-dienes.Distortion dependent intersystem crossing: A femtosecond time-resolved photoelectron spectroscopy study of benzene, toluene, and p-xylene.Energetics of Baird aromaticity supported by inversion of photoexcited chiral [4n]annulene derivatives.Long-range magnetic response of toroidal boron structures: B16 and [Co@B16]-/3- species.Magnetic Response of Aromatic Rings Under Rotation: Aromatic Shielding Cone of Benzene Upon Different Orientations of the Magnetic Field.Aromaticity Reversal in the Lowest Excited Triplet State of Archetypical Möbius Heteroannulenic Systems.Triplet State Aromaticity: NICS Criterion, Hyperconjugation, and Charge Effects.Less stable tautomers form stronger hydrogen bonds: the case of water complexes.Cyclopropyl Group: An Excited-State Aromaticity Indicator?A Description of Vibrational Modes in Hexaphyrins: Understanding the Aromaticity Reversal in the Lowest Triplet State.Triplet state homoaromaticity: concept, computational validation and experimental relevance.

P2860

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P2860

The excited state antiaromatic benzene ring: a molecular Mr Hyde?

http://www.wikidata.org/entity/Q35626497

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

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2015年论文

@zh-cn

name

The excited state antiaromatic benzene ring: a molecular Mr Hyde?

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The excited state antiaromatic benzene ring: a molecular Mr Hyde?

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label

The excited state antiaromatic benzene ring: a molecular Mr Hyde?

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The excited state antiaromatic benzene ring: a molecular Mr Hyde?

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The excited state antiaromatic benzene ring: a molecular Mr Hyde?

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The excited state antiaromatic benzene ring: a molecular Mr Hyde?

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P1433

Chemical Society Reviews

P1476

The excited state antiaromatic benzene ring: a molecular Mr Hyde?

@en

P2093

Henrik Ottosson

http://www.w3.org/2001/XMLSchema#string

P2860

Photohydration and photosolvolysis of biphenyl alkenes and alcohols via biphenyl quinone methide-type intermediates and diarylmethyl carbocations.

Photoaddition of water and alcohols to the anthracene moiety of 9-(2'-hydroxyphenyl)anthracene via formal excited state intramolecular proton transfer.

Binol quinone methides as bisalkylating and DNA cross-linking agents.

Methoxy-substituted stilbenes, styrenes, and 1-arylpropenes: photophysical properties and photoadditions of alcohols.

Photogenerated quinone methides as useful intermediates in the synthesis of chiral BINOL ligands.

Photochemistry of bromofluorobenzenes.

Photochemical generation and the reactivity of o-naphthoquinone methides in aqueous solutions.

Aromaticity effects on the profiles of the lowest triplet-state potential-energy surfaces for rotation about the C=C bonds of olefins with five-membered ring substituents: an example of the impact of Baird's rule.

Near-visible light generation of a quinone methide from 3-hydroxymethyl-2-anthrol.

The arene-alkene photocycloaddition

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6472-6493

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scholarly article

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10.1039/C5CS00057B

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18

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44

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Raffaello Papadakis

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2015-05-11T00:00:00Z

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25960203

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