Affiliation:
1. Department: Department of Applied Chemistry Graduate School of Engineering Institution: Osaka Metropolitan University 1-1 Gakuen-cho, Nakaku Sakai Osaka 599-8531 Japan
2. Department: The Research Institute for Molecular Electronic Devices (RIMED) Institution: Osaka Metropolitan University 1-1 Gakuen-cho, Nakaku Sakai Osaka 599-8531 Japan
Abstract
Abstract2‐(3,6‐Bis(4‐methoxyphenyl)‐2,2,5,5‐tetramethyl‐4‐oxo‐4,5‐dihydropentalen‐1(2H)‐ylidene)malononitrile (DPM‐An) and 2,2′‐(3,6‐bis(4‐methoxyphenyl)‐2,2,5,5‐tetramethyl‐2,5‐dihydropentalene‐1,4‐diylidene)dimalononitrile (DPD‐An), both bearing the 2,5‐dihydropentalene core and intramolecular electron donor–acceptor moieties, were prepared and subjected to photophysical studies. The absorption spectra of DPM‐An and DPD‐An in CH2Cl2 at room temperature contain maxima at similar wavelengths of 406 and 409 nm, respectively. These substances do not luminesce in CH2Cl2 solution at room temperature, but they do emit light when present in poly(methyl methacrylate) films. Interestingly, DPM‐An and DPD‐An in the film forms display nearly identical emission (EM) spectra with respective maxima at 592 and 594 nm. In contrast, DPD‐An has a longer EM lifetime than does DPM‐An. Therefore, the dihydropentalene derivatives, exemplified by DPM‐An and DPD‐An, may be a family of substances in which excited state decay rate can be varied without changing EM wavelengths.
Funder
Hokkaido University
Konica Minolta Imaging Science Foundation