Pyrrolopyrrole aza-BODIPY analogues: A facile synthesis and intense fluorescence

Soji Shimizu; Taku Iino; Yasuyuki Araki; Nagao Kobayashi

doi:10.1039/c3cc38452g

Pyrrolopyrrole aza-BODIPY analogues: A facile synthesis and intense fluorescence

Soji Shimizu, Taku Iino, Yasuyuki Araki, Nagao Kobayashi

Research output: Contribution to journal › Article › peer-review

115 Citations (Scopus)

Abstract

Pyrrolopyrrole aza-BODIPY analogues were synthesized from diketopyrrolopyrrole and heteroaromatic amines in the presence of titanium tetrachloride. These novel compounds exhibit intense absorption in the visible region and strong emission with high fluorescence quantum yields greater than 0.8.

Original language	English
Pages (from-to)	1621-1623
Number of pages	3
Journal	Chemical Communications
Volume	49
Issue number	16
DOIs	https://doi.org/10.1039/c3cc38452g
Publication status	Published - Jan 29 2013
Externally published	Yes

All Science Journal Classification (ASJC) codes

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
Chemistry(all)
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

Access to Document

10.1039/c3cc38452g

Cite this

@article{3bf82e279f754b70bdaa454f0c05ac17,

title = "Pyrrolopyrrole aza-BODIPY analogues: A facile synthesis and intense fluorescence",

abstract = "Pyrrolopyrrole aza-BODIPY analogues were synthesized from diketopyrrolopyrrole and heteroaromatic amines in the presence of titanium tetrachloride. These novel compounds exhibit intense absorption in the visible region and strong emission with high fluorescence quantum yields greater than 0.8.",

author = "Soji Shimizu and Taku Iino and Yasuyuki Araki and Nagao Kobayashi",

year = "2013",

month = jan,

day = "29",

doi = "10.1039/c3cc38452g",

language = "English",

volume = "49",

pages = "1621--1623",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "16",

}

TY - JOUR

T1 - Pyrrolopyrrole aza-BODIPY analogues

T2 - A facile synthesis and intense fluorescence

AU - Shimizu, Soji

AU - Iino, Taku

AU - Araki, Yasuyuki

AU - Kobayashi, Nagao

PY - 2013/1/29

Y1 - 2013/1/29

N2 - Pyrrolopyrrole aza-BODIPY analogues were synthesized from diketopyrrolopyrrole and heteroaromatic amines in the presence of titanium tetrachloride. These novel compounds exhibit intense absorption in the visible region and strong emission with high fluorescence quantum yields greater than 0.8.

AB - Pyrrolopyrrole aza-BODIPY analogues were synthesized from diketopyrrolopyrrole and heteroaromatic amines in the presence of titanium tetrachloride. These novel compounds exhibit intense absorption in the visible region and strong emission with high fluorescence quantum yields greater than 0.8.

UR - http://www.scopus.com/inward/record.url?scp=84873299414&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84873299414&partnerID=8YFLogxK

U2 - 10.1039/c3cc38452g

DO - 10.1039/c3cc38452g

M3 - Article

C2 - 23338046

AN - SCOPUS:84873299414

SN - 1359-7345

VL - 49

SP - 1621

EP - 1623

JO - Chemical Communications

JF - Chemical Communications

IS - 16

ER -

Pyrrolopyrrole aza-BODIPY analogues: A facile synthesis and intense fluorescence

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this