Triplet states of copper and metal-free phthalocyanines

Triplet states of copper and metal-free phthalocyanines
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铜和不含金属的酞菁的三重态

DOI:
10.1039/f29787401870
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发表时间:
1978
期刊:
Journal of the Chemical Society, Faraday Transactions
影响因子:
--
通讯作者:
T. Truscott
T. Truscott
中科院分区:
--
文献类型:
--
作者:
J. Mcvie;R. S. Sinclair;T. Truscott

文献摘要

被引文献

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用激光闪光光解法研究了无金属酞菁(H_2Pc)和酞菁铜(CuPc)在氯代萘稀溶液(10~(-6)mol dm~(-3))中的三重态。对CuPc三重态的首次观察表明,它的寿命非常短(约35 ns),但三重态形成的量子效率(0.70)大于H2Pc(约0.14)。两种化合物的三重态吸收最大值均出现在λ 480 nm处,但CuPc的三重态能级(150 kJ)高于H2Pc的三重态能级(120 kJ)。(10~(-4)~10~(-5)mol dm~(-3))的两种酞菁分别产生短寿命(100 ns)和长寿命(100 ns)的荧光(2.5 µ s)瞬变,这归因于分散在氯萘中的微晶颗粒中激子的形成。
Laser flash photolysis has been used to characterise the triplet state of metal-free (H2Pc) and copper phthalocyanine (CuPc) in dilute (10–6 mol dm–3) solution in chloronaphthalene. This first observation of the triplet state of CuPc indicates that its lifetime is very short (∼35 ns), but the quantum efficiency of triplet formation ( 0.70) is greater than that for H2Pc (∼0.14). The triplet absorption maximum for both compounds occur at ≈480 nm, but the triplet energy level of CuPc (150 kJ) is higher than that for H2Pc (120 kJ).More concentrated solutions (10–4-10–5 mol dm–3) of both phthalocyanines give short-lived (100 ns) and long-lived (2.5 µs) transients, which have been attributed to the formation of excitons in microcrystalline particles dispersed in the chloronaphthalene.