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Photoinduced Charge Separation Promoted by Ring Opening of a Piperazine Radical Cation

NIAID Data Ecosystem2026-03-06 收录

数据链接：

https://figshare.com/articles/dataset/Photoinduced_Charge_Separation_Promoted_by_Ring_Opening_of_a_Piperazine_Radical_Cation/3658791 数据链接链接失效反馈

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资源简介：

Photoinduced Charge Separation Promoted by Ring Opening of a Piperazine Radical Cation

应用场景：

创建时间：

2016-08-18

分子内电荷转移

光诱导电荷转移

A pair of donor−bridge−acceptor electron-transfer complexes, with a carbazole donor and a naphthalimide acceptor connected by either a para- or meta-conjugated phenylacetylene bridge, are synthesized

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Presence and Absence of Excited State Intramolecular Charge Transfer with the Six Isomers of Dicyano- N , N -dimethylaniline and Dicyano-( N -methyl- N -isopropyl)aniline

激发态动力学

光诱导电荷转移

The excited state behavior of the six m,n-dicyano-N,N-dimethylanilines (mnDCDMA) and m,n-dicyano-(N-methyl-N-isopropyl)anilines (mnDCMIA) is discussed as a function of solvent polarity and temperature

NIAID Data Ecosystem50

Synthesis of Dibenzo[ b , f ]silepins with a Benzoquinolyl Ligand

有机硅发光材料

光诱导电荷转移

A benzo[h]quinolyl ligand provided pentacoordinate character for silicon in dibenzo[b,f]silepins. Substituents on the silicon center determined both conformations of the dibenzosilepin and luminescenc

NIAID Data Ecosystem40

Impact of the 2,2′-Bithienyl Framework on the Charge-Transfer Emission of Triarylborane-Based o,o′-Substituted Biaryls

有机光电材料

光诱导电荷转移

Two new triarylborane-based o,o′-substituted 2,2′-bithienyls, BT-BNMe2 and BT-BNBn2, which contain BMes2 and NMe2/NBn2 groups at the 3,3′-positions, have been synthesized. Similar to the o,o′-substitu

NIAID Data Ecosystem60

Counterion Migration Driven by Light-Induced Intramolecular Charge Transfer

光诱导电荷转移

抗衡离子迁移动力学

A series of D−π–A+ pyridinium compounds, in which D = −NPh2 and A+ = −PyMe+ are linked by various amounts of linear phenyl spacers, were strategically designed and synthesized. Their characterization

NIAID Data Ecosystem50

Photoinduced Charge Separation Promoted by Ring Opening of a Piperazine Radical Cation

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