Carbazole Substituted BODIPYs.

Szczegóły
Abstrakt

Tytuł:: Carbazole Substituted BODIPYs.
Autorzy:: Gupta I; Department of Chemistry, Indian Institute of Technology Gandhinagar, Gandhinagar, India.
Kesavan PE; Department of Chemistry, Indian Institute of Technology Gandhinagar, Gandhinagar, India.
Źródło:: Frontiers in chemistry [Front Chem] 2019 Dec 10; Vol. 7, pp. 841. Date of Electronic Publication: 2019 Dec 10 (Print Publication: 2019).
Typ publikacji:: Journal Article; Review
Język:: English
Imprint Name(s):: Original Publication: Lausanne : Frontiers Media S.A., [2013]-
References:: Dalton Trans. 2019 Jun 11;48(23):8488-8501. (PMID: 31116199)
Chem Soc Rev. 2013 Jan 21;42(2):622-61. (PMID: 23093107)
Phys Chem Chem Phys. 2013 Apr 7;15(13):4666-76. (PMID: 23435838)
Analyst. 2018 Oct 22;143(21):5218-5224. (PMID: 30270379)
Chem Soc Rev. 2014 May 21;43(10):3342-405. (PMID: 24577078)
Biomaterials. 2014 Jul;35(23):6078-85. (PMID: 24794926)
Chem Soc Rev. 2015 Jul 21;44(14):4953-72. (PMID: 25801415)
Analyst. 2017 Feb 14;142(4):603-607. (PMID: 28138671)
Chem Soc Rev. 2013 Jan 7;42(1):29-43. (PMID: 23059554)
Chem Soc Rev. 2014 Jul 7;43(13):4778-823. (PMID: 24733589)
ACS Nano. 2018 Aug 28;12(8):8145-8159. (PMID: 30074773)
Chem Soc Rev. 2013 Jan 7;42(1):77-88. (PMID: 23014776)
Dalton Trans. 2016 Feb 14;45(6):2700-8. (PMID: 26743311)
J Fluoresc. 2017 Nov;27(6):2131-2144. (PMID: 28808835)
Luminescence. 2018 Feb;33(1):10-14. (PMID: 28681566)
J Med Chem. 2018 May 10;61(9):3952-3961. (PMID: 29681157)
J Org Chem. 2018 May 4;83(9):5274-5281. (PMID: 29634267)
Phys Chem Chem Phys. 2015 Jul 14;17(26):17221-36. (PMID: 26074136)
Chem Rev. 2010 May 12;110(5):2795-838. (PMID: 20353192)
Phys Chem Chem Phys. 2015 Oct 28;17(40):26580-8. (PMID: 26394373)
Bioorg Chem. 2019 Oct;91:103139. (PMID: 31369976)
Org Biomol Chem. 2014 Jun 21;12(23):3774-91. (PMID: 24781214)
Phys Chem Chem Phys. 2018 Nov 7;20(43):27418-27428. (PMID: 30357210)
Sci Rep. 2017 May 9;7(1):1611. (PMID: 28487525)
Dalton Trans. 2014 Sep 14;43(34):13076-86. (PMID: 25043199)
Chem Rev. 2007 Nov;107(11):4891-932. (PMID: 17924696)
Angew Chem Int Ed Engl. 2008;47(7):1184-201. (PMID: 18092309)
Org Lett. 2015 Jun 19;17(12):3090-3. (PMID: 26053127)
Dalton Trans. 2015 Oct 21;44(39):17209-21. (PMID: 26373792)
Org Lett. 2010 Apr 2;12(7):1464-7. (PMID: 20210334)
Dalton Trans. 2014 Aug 28;43(32):12405-13. (PMID: 24999586)
Photochem Photobiol. 2015 May-Jun;91(3):637-53. (PMID: 25683093)
Org Biomol Chem. 2015 Mar 7;13(9):2501-17. (PMID: 25594728)
J Org Chem. 2013 Sep 20;78(18):9153-60. (PMID: 23984818)
Chemistry. 2016 May 23;22(22):7508-13. (PMID: 27072791)
Chemistry. 2017 May 11;23(27):6570-6578. (PMID: 28226192)
Chem Rev. 2015 Aug 12;115(15):7893-943. (PMID: 25965103)
Dalton Trans. 2013 Feb 14;42(6):2062-74. (PMID: 23178459)
Chem Rev. 2007 May;107(5):1831-61. (PMID: 17430001)
J Org Chem. 2008 Sep 5;73(17):6513-20. (PMID: 18666796)
Dalton Trans. 2015 Sep 28;44(36):15803-12. (PMID: 25812138)
Chem Soc Rev. 2012 Feb 7;41(3):1130-72. (PMID: 21796324)
Chem Commun (Camb). 2019 Mar 7;55(21):3136-3139. (PMID: 30794277)
J Am Chem Soc. 2016 Nov 9;138(44):14586-14591. (PMID: 27786443)
Chem Asian J. 2016 May 20;11(10):1572-87. (PMID: 26918806)
Chem Commun (Camb). 2012 Sep 14;48(71):8913-5. (PMID: 22842497)
Org Lett. 2011 Nov 18;13(22):6030-3. (PMID: 22029570)
Phys Chem Chem Phys. 2017 Aug 23;19(33):22049-22060. (PMID: 28792028)
Chem Cent J. 2018 May 11;12(1):60. (PMID: 29748728)
Eur J Med Chem. 2015 Apr 13;94:405-26. (PMID: 25794500)
Chem Commun (Camb). 2018 Aug 14;54(66):9123-9126. (PMID: 30010163)
ACS Appl Mater Interfaces. 2017 Nov 22;9(46):39873-39889. (PMID: 29072443)
Org Biomol Chem. 2017 Nov 15;15(44):9283-9287. (PMID: 29039863)
Contributed Indexing:: Keywords: BODIPY; absorption; carbazole; dyes; fluorescence
Entry Date(s):: Date Created: 20200111 Latest Revision: 20200930
Update Code:: 20240105
PubMed Central ID:: PMC6914821
DOI:: 10.3389/fchem.2019.00841
PMID:: 31921766
: Czasopismo naukowe

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Difluoroboron-dipyrromethenes (BODIPYs) are highly popular fluorescent dyes with applications as NIR probes for bioimaging, fluorescent tags/sensors and as photosensitizers in cancer therapy and organic photovoltaics. This review concentrates on the synthesis and spectral properties of BODIPY dyes conjugated with carbazole heterocycle. The carbazole is an electron rich tricyclic compound and due to its excellent electronic properties, it is extensively used in the production of electroluminescent materials and polymers. This review highlights the recent progress made on the series of BODIPY derivatives containing carbazole ring at alpha, beta , and meso -positions of the BODIPY skeleton. Carbazole based hybrid BODIPYs, carbazole linked aza-BODIPYs and carbazole-fused BODIPYs are also discussed.
(Copyright © 2019 Gupta and Kesavan.)

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