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丁二炔连接的双(咪唑基卟啉)自组装体的双光子吸收特性

Two-photon absorption properties of self-assemblies of butadiyne-linked bis(imidazolylporphyrin).

作者信息

Ogawa Kazuya, Ohashi Atsushi, Kobuke Yoshiaki, Kamada Kenji, Ohta Koji

机构信息

Graduate School of Materials Science, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0101, Japan.

出版信息

J Phys Chem B. 2005 Nov 24;109(46):22003-12. doi: 10.1021/jp054444z.

Abstract

Supramolecular porphyrin self-assemblies have been prepared from butadiyne-linked bis(imidazolylporphyrin) by complementary coordination of imidazole to zinc, and their two-photon absorption (2PA) and higher-order nonlinear absorption properties were investigated over femtosecond time scales using an open-aperture Z-scan method. The self-assembled porphyrin dimer of the conjugated monozinc bisporphyrin 7D was shown to have a large 2PA cross section (7.6 x 10(3) GM, where 1 GM = 10(-50) cm(4) s molecule(-1) photon(-1)) at 887 nm. By comparison of this result with that for a meso-meso-linked porphyrin array without the butadiyne connection (3.7 x 10(2) GM at 964 nm), it was demonstrated that the predominant factor in this significant enhancement of the cross section was the expansion of porphyrin-porphyrin pi-conjugation. Self-coordination and monozinc metalation were also found to be contributing factors. Furthermore, a novel self-assembled porphyrin polymer 8P consisting of a biszinc complex with a mean molecular weight of M(n) = 1.5 x 10(5) Da was shown to exhibit an extraordinarily large two-photon absorption cross section (4.4 x 10(5) GM at 873 nm). Nanosecond Z-scan experiments for 7D and 8P were also undertaken and resulted in the measurement of large effective 2PA cross sections, including the excited-state absorption (2.1 x 10(5) GM for 7D and 2.2 x 10(7) GM for 8P, respectively). Finally, three-photon absorption was observed by femtosecond Z-scan experiments at 1188 nm (7.1 x 10(-89) m(6) s(2)) and 1282 nm (1.8 x 10(-89) m(6) s(2)), an observation which is the first of its kind in porphyrin chemistry.

摘要

通过咪唑与锌的互补配位作用,由丁二炔连接的双(咪唑基卟啉)制备了超分子卟啉自组装体,并使用开孔Z扫描方法在飞秒时间尺度上研究了它们的双光子吸收(2PA)和高阶非线性吸收特性。共轭单锌双卟啉7D的自组装卟啉二聚体在887 nm处显示出较大的2PA截面(7.6×10³ GM,其中1 GM = 10⁻⁵⁰ cm⁴ s molecule⁻¹ photon⁻¹)。通过将该结果与没有丁二炔连接的中位-中位连接卟啉阵列的结果(在964 nm处为3.7×10² GM)进行比较,证明了截面显著增强的主要因素是卟啉-卟啉π共轭的扩展。还发现自配位和单锌金属化是促成因素。此外,一种由平均分子量M(n) = 1.5×10⁵ Da的双锌配合物组成的新型自组装卟啉聚合物8P在873 nm处显示出极大的双光子吸收截面(4.4×10⁵ GM)。还对7D和8P进行了纳秒Z扫描实验,结果测量到了较大的有效2PA截面,包括激发态吸收(7D分别为2.1×10⁵ GM,8P为2.2×10⁷ GM)。最后,通过飞秒Z扫描实验在1188 nm(7.1×10⁻⁸⁹ m⁶ s²)和1282 nm(1.8×10⁻⁸⁹ m⁶ s²)处观察到了三光子吸收,这一观察结果在卟啉化学中尚属首次。

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