Literature DB >> 21548624

Luminescent charge-transfer complexes: tuning emission in binary fluorophore mixtures.

Maneesh D Gujrati1, N S Saleesh Kumar, Adrienne S Brown, Burjor Captain, James N Wilson.   

Abstract

Charge-transfer (CT) complexes composed of a π-electron-poor naphthalene diimide (NDI) derivative combined with a series of π-electron-rich donors were investigated. Solutions of the CT complexes are nonemissive; however, solid-state complexes and aqueous suspensions display emission that is dependent on the energy of the HOMO of the electron donor. Crystallographic analysis of a pyrene-NDI complex reveals columnar packing and a high degree of frontier molecular orbital (FMO) overlap that likely contributes to the observed optical properties. The fluorescent CT particles are utilized as imaging agents; additional luminescent CT complexes may be realized by considering FMO energies and topologies.

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Year:  2011        PMID: 21548624     DOI: 10.1021/la2012809

Source DB:  PubMed          Journal:  Langmuir        ISSN: 0743-7463            Impact factor:   3.882


  3 in total

1.  Tuning the donor-acceptor interactions in phase-segregated block molecules.

Authors:  Brigitte A G Lamers; Martin H C van Son; Freek V de Graaf; Bart W L van den Bersselaar; Bas F M de Waal; Kazuki Komatsu; Hiroshi Sato; Takuzo Aida; José Augusto Berrocal; Anja R A Palmans; Ghislaine Vantomme; Stefan C J Meskers; E W Meijer
Journal:  Mater Horiz       Date:  2022-01-04       Impact factor: 13.266

2.  Adaptive molecular quaternary clips made with pyrene functionalized polyhedral oligomeric silsesquioxane.

Authors:  Tsung-Kai Yang; Jou-Tsen Ou; Heng-Yi Lin; Wei-Cheng Peng; Meng-Hsuan Jao; Jia Chen; Bin Sun; Yu Zhu; Chien-Lung Wang
Journal:  Nanoscale Adv       Date:  2020-11-11

3.  Molecular assembly of amino acid interlinked, topologically symmetric, π-complementary donor-acceptor-donor triads.

Authors:  M B Avinash; K V Sandeepa; T Govindaraju
Journal:  Beilstein J Org Chem       Date:  2013-08-01       Impact factor: 2.883

  3 in total

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