Results 21 to 30 of about 32,802 (321)

Carbazole Substituted BODIPYs [PDF]

open access: yesFrontiers in Chemistry, 2019
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
Iti Gupta, Praseetha E. Kesavan
openaire   +3 more sources

Highly efficient multilayer organic pure-blue-light emitting diodes with substituted carbazoles compounds in the emitting layer [PDF]

open access: yes, 2006
Bright blue organic light-emitting diodes (OLEDs) based on 1,4,5,8,N-pentamethylcarbazole (PMC) and on dimer of N-ethylcarbazole (N,N'-diethyl-3,3'-bicarbazyl) (DEC) as emitting layers or as dopants in a 4,4'-bis(2,2'-diphenylvinyl)-1,1'-biphenyl (DPVBi)
A Fischer   +9 more
core   +4 more sources

Brønsted Acid-Catalyzed Straightforward Synthesis of Benzo[b]carbazoles from 2,3-Unsubstituted Indoles [PDF]

open access: yes, 2014
Described is a general and efficient synthesis of valuable benzo[b]carbazoles by Brønsted acid-catalyzed reactions between simple C-2,C-3-unsubstituted indoles and ortho-[α-(hydroxy)benzyl]benzaldehyde acetals.
Appukkuttan   +48 more
core   +1 more source

Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review

open access: yesMolecules, 2015
Carbazoles represent an important class of heterocycles. These have been reported to exhibit diverse biological activities such as antimicrobial, antitumor, antiepileptic, antihistaminic, antioxidative, anti-inflammatory, antidiarrhoeal, analgesic ...
Maryam Bashir   +3 more
doaj   +1 more source

Recent Advances in the Biosynthesis of Carbazoles Produced by Actinomycetes

open access: yesBiomolecules, 2020
Structurally diverse carbazole alkaloids are valuable due to their pharmaceutical properties and have been isolated from nature. Experimental knowledge on carbazole biosynthesis is limited. The latest development of in silico analysis of the biosynthetic
Masaya Kobayashi, Tomohisa Kuzuyama
doaj   +1 more source

Iodine recycling via 1,3-migration in iodoindoles under metal catalysis [PDF]

open access: yes, 2013
3-Substituted (indol-2-yl)-α-allenols show divergent patterns of reactivity under metal catalysis. An unprecedented intramolecular 1,3-iodine migration is described.
Alcaide, Benito   +6 more
core   +2 more sources

9-[3-(Carbazol-9-yl)-5-methylphenyl]carbazole [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2013
The title compound, C31H22N2, crystallizes with two symmetry-independent mol-ecules in the asymmetric unit. The mol-ecules have slightly different conformations, the dihedral angles between the central phenyl ring and the carbazolyl groups being 56.29 (4) and 59.57 (4)° in one mol-ecule and 48.71 (4) and 65.47 (4)° in the other.
Jae Eun Kim   +3 more
openaire   +3 more sources

Carbazole based organic dyes as effective photosensitizers: A comprehensive analysis of their structure‐property relationships

open access: yesElectrochemical Science Advances, 2022
The present work describes the effect of structural modification of carbazole‐based photosensitizers carrying carboxylic acid as a common anchoring functionality, on the photovoltaic parameters of newly fabricated DSSCs.
Praveen Naik   +4 more
doaj   +1 more source

Use of Phenyl Formate as a CO Surrogate for the Reductive Cyclization of Organic Nitro Compounds to Yield Different N-Heterocycles: Avoiding the Use of Autoclaves and Pressurized Gases

open access: yesChemistry Proceedings, 2022
The reductive cyclization of different organic nitro compounds by carbon monoxide, catalyzed by transition metal complexes, is a very efficient and clean strategy for the synthesis of many N-heterocycles.
Fabio Ragaini   +2 more
doaj   +1 more source

Molecular Orientations of Delayed Fluorescent Emitters in a Series of Carbazole-Based Host Materials

open access: yesFrontiers in Chemistry, 2020
Molecular orientation is one of the most crucial factors to boost the efficiency of organic light-emitting devices. However, active control of molecular orientation of the emitter molecule by the host molecule is rarely realized so far, and the ...
Hisahiro Sasabe   +16 more
doaj   +1 more source

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