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A push–pull unsymmetrical subphthalocyanine dimer

descriptionPublicationkeyboard_double_arrow_right Article , Other literature type 01 Jan 2015 Germany, Spain, United Kingdom, Spain English Publisher:Royal Society of Chemistry (RSC)Journal:Chemical Science, volume 6, pages 5,571-5,577 (issn: 2041-6520, eissn: 2041-6539, Copyright policy )Funded by:DFG | unidentified
Authors: Germán Zango; Johannes Zirzlmeier; Christian G. Claessens; Timothy Clark; M. Victoria Martínez-Díaz; Dirk M. Guldi; Tomás Torres;

doi: 10.1039/c5sc01709b

pmid: 29861894

pmc: PMC5949859

handle: 10486/671021 , 20.500.12614/1107

A push–pull unsymmetrical subphthalocyanine dimer

Abstract

Unsymmetrical subphthalocyanine fused dimers have been prepared, resulting in unprecedented push–pull π-extended curved aromatic macrocycles.

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Keywords

/dk/atira/pure/core/subjects/pharmacy, Electron acceptor, Electrons, Charge transfer state, Pharmacy, Química, Fluorescence, WNU, Chemistry, Charge transfer, DDC Classification::5 Naturwissenschaften und Mathematik :: 54 Chemie :: 540 Chemie und zugeordnete Wissenschaften, Steel beams and girders, Dimers

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selected citations
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
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