Literature DB >> 23014353

Size-dependent fluorescence properties of [n]cycloparaphenylenes (n = 8-13), hoop-shaped π-conjugated molecules.

Mamoru Fujitsuka1, Dae Won Cho, Takahiro Iwamoto, Shigeru Yamago, Tetsuro Majima.   

Abstract

Hoop-shaped π-conjugated molecules such as cycloparaphenylene (CPP) have attracted the attention of many chemists because they exhibit interesting properties due to the distorted π-electron system. To gain a systematic understanding of the properties that result from distorted π-electron systems, it is important to know precisely how these properties depend on the hoop size. In the present study, we have investigated the size dependence of the fluorescence properties of CPPs. The fluorescence spectra of smaller CPPs showed red-shifted fluorescence peaks, smaller fluorescence quantum yields, and longer lifetimes, when compared to those of larger ones. One of the important factors that gave rise to these fluorescence properties of smaller CPPs was greater structural relaxation from the Franck-Condon state, which is a postulation supported by theoretical calculations. The structural relaxation in the picosecond domain was experimentally detected by the fluorescence upconversion method. The present results are an important example that confirms steric factors strongly governing the fluorescence properties of a molecule.

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Year:  2012        PMID: 23014353     DOI: 10.1039/c2cp42712e

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  9 in total

1.  Efficient room-temperature synthesis of a highly strained carbon nanohoop fragment of buckminsterfullerene.

Authors:  Paul J Evans; Evan R Darzi; Ramesh Jasti
Journal:  Nat Chem       Date:  2014-03-09       Impact factor: 24.427

2.  Spatial separation of triplet excitons drives endothermic singlet fission.

Authors:  Nadezhda V Korovina; Christopher H Chang; Justin C Johnson
Journal:  Nat Chem       Date:  2020-03-02       Impact factor: 24.427

3.  Perfluorocycloparaphenylenes.

Authors:  Hiroki Shudo; Motonobu Kuwayama; Masafumi Shimasaki; Taishi Nishihara; Youhei Takeda; Nobuhiko Mitoma; Takuya Kuwabara; Akiko Yagi; Yasutomo Segawa; Kenichiro Itami
Journal:  Nat Commun       Date:  2022-06-28       Impact factor: 17.694

4.  Synthesis and properties of [8]-, [10]-, [12]-, and [16]cyclo-1,4-naphthylenes.

Authors:  Keishu Okada; Akiko Yagi; Yasutomo Segawa; Kenichiro Itami
Journal:  Chem Sci       Date:  2016-09-12       Impact factor: 9.825

5.  Cycloparaphenylene as a molecular porous carbon solid with uniform pores exhibiting adsorption-induced softness.

Authors:  Hirotoshi Sakamoto; Toshihiko Fujimori; Xiaolin Li; Katsumi Kaneko; Kai Kan; Noriaki Ozaki; Yuh Hijikata; Stephan Irle; Kenichiro Itami
Journal:  Chem Sci       Date:  2016-03-09       Impact factor: 9.825

6.  Linear, Non-Conjugated Cyclic and Conjugated Cyclic Paraphenylene under Pressure.

Authors:  Miriam Peña-Álvarez; Samuele Fanetti; Naomi Falsini; Giulia Novelli; Juan Casado; Valentín G Baonza; Mercedes Taravillo; Simon Parsons; Roberto Bini; Margherita Citroni
Journal:  Molecules       Date:  2019-09-26       Impact factor: 4.411

Review 7.  Nano-rings with a handle - Synthesis of substituted cycloparaphenylenes.

Authors:  Anne-Florence Tran-Van; Hermann A Wegner
Journal:  Beilstein J Nanotechnol       Date:  2014-08-20       Impact factor: 3.649

8.  Carbon nanorings with inserted acenes: breaking symmetry in excited state dynamics.

Authors:  R Franklin-Mergarejo; D Ondarse Alvarez; S Tretiak; S Fernandez-Alberti
Journal:  Sci Rep       Date:  2016-08-10       Impact factor: 4.379

Review 9.  Conjugated Nanohoops Incorporating Donor, Acceptor, Hetero- or Polycyclic Aromatics.

Authors:  Mathias Hermann; Daniel Wassy; Birgit Esser
Journal:  Angew Chem Int Ed Engl       Date:  2021-03-22       Impact factor: 16.823

  9 in total

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