Analysis on high-resolution spectrum of the S1–S0 transition of free-base phthalocyanine

Author:

Miyamoto Yuki1ORCID,Hiramoto Ayami1ORCID,Iwakuni Kana2ORCID,Kuma Susumu3ORCID,Enomoto Katsunari4ORCID,Nakayama Naofumi5ORCID,Baba Masaaki67ORCID

Affiliation:

1. Research Institute for Interdisciplinary Science, Okayama University 1 , Kita-ku, Okayama 700-8530, Japan

2. Institute for Laser Science, University of Electro-Communications 2 , Chofu, Tokyo 182-8585, Japan

3. Atomic, Molecular and Optical Physics Laboratory, RIKEN 3 , Wako, Saitama 351-0198, Japan

4. Department of Physics, University of Toyama 4 , Toyama 930-8555, Japan

5. CONFLEX Corporation 5 , 3-23-17 Takanawa, Minato-ku, Tokyo 108-0074, Japan

6. Molecular Photoscience Research Center, Kobe University 6 , Kobe 657-8501, Japan

7. Division of Chemistry, Graduate School of Science, Kyoto University 7 , Kyoto 606-8502, Japan

Abstract

A high-resolution absorption spectrum of the S1–S0 transition of free-base phthalocyanine was observed and analyzed with improved reliability. The spectrum, with a partially resolved rotational structure, was obtained by using the buffer-gas cooling technique and a single-mode tunable laser. Our new analysis reveals that the S1←S0000 band belongs to the a-type transition, where the electronic transition moment aligns parallel to the NH–HN direction, allowing the assignment of the S1 state to 1B3u. These results agree with a prior study using supersonic expansion and are well supported by theoretical calculations. Interestingly, the rotational constant B in the S1 state, which is often smaller than that in the ground state for typical molecules, was found to be slightly larger than that in the S01Ag state. This suggests a change in the character of π bonds with the electronic excitation.

Funder

Japan Society for the Promotion of Science

Publisher

AIP Publishing

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