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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >THE OCTAETHYLPORPHYRIN-DIHEXYLBITHIOPHENE DERIVATIVES COMBINED WITH PYRIDINE AND PYRIMIDINE RINGS. THEIR SYNTHESES AND PROTON-MEDIATED AND HEAT-DRIVEN SPECTRAL CHANGES
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THE OCTAETHYLPORPHYRIN-DIHEXYLBITHIOPHENE DERIVATIVES COMBINED WITH PYRIDINE AND PYRIMIDINE RINGS. THEIR SYNTHESES AND PROTON-MEDIATED AND HEAT-DRIVEN SPECTRAL CHANGES

机译:与吡啶环和嘧啶环组合的八烷基卟啉-二己基苯并菲衍生物。它们的合成以及质子介导和热驱动的光谱变化

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摘要

The octaethylporphyrin (OEP)-dihexylbithiophene (DHBTh) derivatives combined with pyridine (Pyr) and pyrimidine (Pym) as proton-acceptable rings (PAR) were synthesized, describable as OEP-DHBTh-PAR, in which all the OEP, DHBTh, and PAR components are connected with diacetylene linkage. Their ~1H NMR and electronic spectral properties and electrochemical behaviors were studied under the neutral and acidic conditions. Reversible proton-mediated and heat-driven spectral changes of OEP- DHBTh-PAR were performed, reflecting both properties of PAR and DHBTh.
机译:合成了八乙基卟啉(OEP)-二己基联噻吩(DHBTh)衍生物与吡啶(Pyr)和嘧啶(Pym)结合作为质子可接受的环(PAR),描述为OEP-DHBTh-PAR,其中所有OEP,DHBTh和PAR组分通过联乙炔键连接。在中性和酸性条件下研究了它们的〜1H NMR和电子光谱性质以及电化学行为。进行了OEP-DHBTh-PAR的可逆质子介导和热驱动光谱变化,反映了PAR和DHBTh的性质。

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