Doubly meso‐β‐Linked Diporphyrins from Oxidation of 5,10,15‐Triaryl‐Substituted NiII– and PdII – Porphyrins

Doubly meso‐β‐Linked Diporphyrins from Oxidation of 5,10,15‐Triaryl‐Substituted NiII– and PdII – Porphyrins
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5,10,15-三芳基取代的 NiII- 和 PdII- 卟啉氧化产生双内消旋-β-连接二卟啉

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发表时间:
2000
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通讯作者:
A. Osuka
A. Osuka
中科院分区:
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作者:
Akihiko Tsuda;A. Nakano;H. Furuta;H. Yamochi;A. Osuka

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通过用六氯锑酸三(4-溴苯基)铵单电子氧化获得的二卟啉显示出比单体起始材料更低的氧化电位[参见例如Eq.①]。这一点和对产物的Soret带观察到的强红移表明稠合双卟啉中广泛的离域π-电子系统。Ar= 3,5-二叔丁基苯基。
Lower oxidation potentials than for the monomeric starting materials are displayed by the diporphyrins obtained by one-electron oxidation with tris(4-bromophenyl)ammonium hexachloroantimonate [see, for example, Eq. (1)]. This and the strong red shift observed for the Soret bands of the product are indicative of extensively delocalized π-electron systems in the fused diporphyrin. Ar=3,5-di-tert-butylphenyl.