Tetracyanobutadiene Bridged Push-Pull Chromophores: Development of New Generation Optoelectronic Materials

Yuvraj Patil; Holger Butenschön; Rajneesh Misra

doi:10.1002/tcr.202200208

Tetracyanobutadiene Bridged Push-Pull Chromophores: Development of New Generation Optoelectronic Materials

Yuvraj Patil
, Holger Butenschön^*
, Rajneesh Misra^*

^*Korrespondierende*r Autor*in für diese Arbeit

Institut für Organische Chemie

Indian Institute of Technology Indore (IITI)

Publikation: Beitrag in Fachzeitschrift › Übersichtsarbeit › Forschung › Peer-Review

Abstract

This review describes the design strategies used for the synthesis of various tetracyanobutadiene bridged donor-acceptor molecular architectures by a click type [2+2] cycloaddition-retroelectrocyclization (CA-RE) reaction sequence. The photophysical and electrochemical properties of the tetracyanobutadiene bridged molecular architectures based on various moieties including diketopyrrolopyrrole, isoindigo, benzothiadiazole, pyrene, pyrazabole, truxene, boron dipyrromethene (BODIPY), phenothiazine, triphenylamine, thiazole and bisthiazole are summarized. Further, we discuss some important applications of the tetracyanobutadiene bridged derivatives in dye sensitized solar cells, bulk heterojunction solar cells and photothermal cancer therapy.

Originalsprache	Englisch
Aufsatznummer	e202200208
Seitenumfang	30
Fachzeitschrift	The chemical record
Jahrgang	23
Ausgabenummer	1
DOIs	https://doi.org/10.1002/tcr.202200208
Publikationsstatus	Veröffentlicht - 19 Jan. 2023

UN-Ziele für nachhaltige Entwicklung (SDGs)

2015 einigten sich die UN-Mitgliedstaaten auf 17 globale Ziele für nachhaltige Entwicklung (Sustainable Development Goals, SDGs) zur Beendigung von Armut, zum Schutz des Planeten und zur Förderung des allgemeinen Wohlstands. Hiermit leisten wir einen Beitrag zu folgendem/n Ziel(en) für nachhaltige Entwicklung (SDGs):

SDG 3 Gute Gesundheit und Wohlergehen

ASJC Scopus Sachgebiete

Allgemeine Chemie
Biochemie
Allgemeine chemische Verfahrenstechnik
Werkstoffchemie

Zugriff auf Dokument

10.1002/tcr.202200208Lizenz: CC BY-NC-ND 4.0

Andere Dateien und Links

Verknüpfung zur Publikation in Scopus

Dieses zitieren

@article{c30842b1d7e647c39ae9737ebe6c7a25,

title = "Tetracyanobutadiene Bridged Push-Pull Chromophores: Development of New Generation Optoelectronic Materials",

abstract = "This review describes the design strategies used for the synthesis of various tetracyanobutadiene bridged donor-acceptor molecular architectures by a click type [2+2] cycloaddition-retroelectrocyclization (CA-RE) reaction sequence. The photophysical and electrochemical properties of the tetracyanobutadiene bridged molecular architectures based on various moieties including diketopyrrolopyrrole, isoindigo, benzothiadiazole, pyrene, pyrazabole, truxene, boron dipyrromethene (BODIPY), phenothiazine, triphenylamine, thiazole and bisthiazole are summarized. Further, we discuss some important applications of the tetracyanobutadiene bridged derivatives in dye sensitized solar cells, bulk heterojunction solar cells and photothermal cancer therapy.",

keywords = "Cycloaddition-retroelectrocyclization, Photothermal Therapy, Solar Cells, Tetracyanoethylene",

author = "Yuvraj Patil and Holger Butensch{\"o}n and Rajneesh Misra",

note = "Funding Information: We thank the and SERB (Project No. CRG/2018/000032), New Delhi, and DAAD (Leibniz University Hannover and IIT Indore project). R. M. thanks the Alexander von Humboldt Foundation for a research fellowship. Open Access funding enabled and organized by Projekt DEAL. New Passage to India ",

year = "2023",

month = jan,

day = "19",

doi = "10.1002/tcr.202200208",

language = "English",

volume = "23",

journal = "The chemical record",

issn = "1527-8999",

publisher = "John Wiley \& Sons Inc.",

number = "1",

}

TY - JOUR

T1 - Tetracyanobutadiene Bridged Push-Pull Chromophores

T2 - Development of New Generation Optoelectronic Materials

AU - Patil, Yuvraj

AU - Butenschön, Holger

AU - Misra, Rajneesh

N1 - Funding Information: We thank the and SERB (Project No. CRG/2018/000032), New Delhi, and DAAD (Leibniz University Hannover and IIT Indore project). R. M. thanks the Alexander von Humboldt Foundation for a research fellowship. Open Access funding enabled and organized by Projekt DEAL. New Passage to India

PY - 2023/1/19

Y1 - 2023/1/19

N2 - This review describes the design strategies used for the synthesis of various tetracyanobutadiene bridged donor-acceptor molecular architectures by a click type [2+2] cycloaddition-retroelectrocyclization (CA-RE) reaction sequence. The photophysical and electrochemical properties of the tetracyanobutadiene bridged molecular architectures based on various moieties including diketopyrrolopyrrole, isoindigo, benzothiadiazole, pyrene, pyrazabole, truxene, boron dipyrromethene (BODIPY), phenothiazine, triphenylamine, thiazole and bisthiazole are summarized. Further, we discuss some important applications of the tetracyanobutadiene bridged derivatives in dye sensitized solar cells, bulk heterojunction solar cells and photothermal cancer therapy.

AB - This review describes the design strategies used for the synthesis of various tetracyanobutadiene bridged donor-acceptor molecular architectures by a click type [2+2] cycloaddition-retroelectrocyclization (CA-RE) reaction sequence. The photophysical and electrochemical properties of the tetracyanobutadiene bridged molecular architectures based on various moieties including diketopyrrolopyrrole, isoindigo, benzothiadiazole, pyrene, pyrazabole, truxene, boron dipyrromethene (BODIPY), phenothiazine, triphenylamine, thiazole and bisthiazole are summarized. Further, we discuss some important applications of the tetracyanobutadiene bridged derivatives in dye sensitized solar cells, bulk heterojunction solar cells and photothermal cancer therapy.

KW - Cycloaddition-retroelectrocyclization

KW - Photothermal Therapy

KW - Solar Cells

KW - Tetracyanoethylene

UR - https://www.scopus.com/pages/publications/85139475496

U2 - 10.1002/tcr.202200208

DO - 10.1002/tcr.202200208

M3 - Review article

AN - SCOPUS:85139475496

SN - 1527-8999

VL - 23

JO - The chemical record

JF - The chemical record

IS - 1

M1 - e202200208

ER -