Tuning the π-bridge of quadrupolar triarylborane chromophores for one- and two-photon excited fluorescence imaging of lysosomes in live cells-Reference-Cited by-同舟云学术

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Tuning the π-bridge of quadrupolar triarylborane chromophores for one- and two-photon excited fluorescence imaging of lysosomes in live cells

Published:2019 Issue:20 Volume:10 Page:5405-5422
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Griesbeck Stefanie¹²³⁴⁵^ORCID,Michail Evripidis⁶³⁴⁵,Wang Chenguang⁷⁸⁹¹⁰,Ogasawara Hiroaki⁷⁸⁹¹⁰^ORCID,Lorenzen Sabine¹²³⁴⁵,Gerstner Lukas¹²³⁴⁵,Zang Theresa¹²³⁴⁵,Nitsch Jörn¹²³⁴⁵^ORCID,Sato Yoshikatsu⁷⁸⁹¹⁰,Bertermann Rüdiger¹²³⁴⁵,Taki Masayasu⁷⁸⁹¹⁰^ORCID,Lambert Christoph⁶³⁴⁵^ORCID,Yamaguchi Shigehiro⁷⁸⁹¹⁰^ORCID,Marder Todd B.¹²³⁴⁵^ORCID

Affiliation:

1. Institut für Anorganische Chemie

2. Institute for Sustainable Chemistry & Catalysis with Boron

3. Julius-Maximilians-Universität Würzburg

4. 97074 Würzburg

5. Germany

6. Institut für Organische Chemie

7. Institute of Transformative Bio-Molecules

8. Nagoya University

9. Nagoya

10. Japan

Abstract

The tetracationic diketopyrrolopyrrole compound 5M exhibits a σ₂ value of 4560 GM at 740 nm.

Funder

Deutsche Forschungsgemeinschaft

Julius-Maximilians-Universität Würzburg

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/SC/C9SC00793H

Reference139 articles.

1. Boron Chemistry Lights the Way: Optical Properties of Molecular and Polymeric Systems C.D.E. thanks EPSRC for a postgraduate studentship and Syngenta for a postgraduate scholarship, and T.B.M. thanks the University of Durham for support and Prof. Dr. K. Tamao for a preprint of ref. 32.

2. Applications of Three-Coordinate Organoboron Compounds and Polymers in Optoelectronics

3. Boron as a key component for new π-electron materials

4. Lewis acidic organoboron polymers

5. A New Design Strategy for Organic Optoelectronic Materials by Lateral Boryl Substitution

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