Results 31 to 40 of about 2,756 (235)

Synthesis of Carbazoles and Derivatives from Allenes

open access: yes, 2022
Carbazole heterocycles are ubiquitous in nature, and frequent motifs in materials such as polymers, dyes and light emitted devices. Among the wide variety of strategies towards the synthesis of carbazoles, the allene-based methodology represents one of
Alonso, José M., Almendros, Pedro
core   +1 more source

Blue Upconversion Organic Light‐Emitting Diodes Achieving 1000 cd m−2 With an Operating Voltage of 2.7 V by Suppressing Interfacial Exciton Quenching

open access: yesAdvanced Functional Materials, EarlyView.
A triplet‐blocking layer controls triplet exciton dynamics in blue upconversion OLEDs. The layer keeps charge transfer (CT)‐generated triplet excitons inside the triplet‐triplet annihilation (TTA) host, suppresses anode‐side interfacial quenching, and increases the steady‐state triplet population.
Qing‐Jun Shui   +5 more
wiley   +1 more source

Role of the Recombination Zone in Organic Light‐Emitting Devices

open access: yesAdvanced Materials, EarlyView.
This review summarizes the critical role of the recombination zone in organic light‐emitting diodes (OLEDs). We highlight that broadening the recombination zone in OLEDs based on emissive layers with balanced charge transport and high photoluminescence quantum yields provides a promising route toward achieving both long operational lifetime and high ...
Yungui Li, Karl Leo
wiley   +1 more source

3-(Trimethylsilylethynyl)carbazole

open access: yesActa Crystallographica Section E Structure Reports Online, 2003
The title compound, [Si(CH3)3(C14H8N)] is a TMS-protected mono-alkyne. It is used as a model species for platinum σ-acetyl­ide compounds of which it is a precursor. Such compounds are of interest due to the extended π-conjugation through the hetero-aromatic linker unit in the backbone.
Khan, M.S.   +4 more
openaire   +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

Visible-Light Photoredox-Catalyzed Three-Component Reaction of Carbazoles with Alkenes and S‑(Difluoromethyl)sulfonium Salt: A Practical Approach to Access Difluoroalkyl-Functionalized Carbazoles

open access: yes, 2023
A mild and elegant multicomponent protocol for construction of CF2H-containing carbazoles was accomplished by visible-light photoredox catalysis with formation of two new C–C bonds in a single step to deliver a wide variety of structurally diverse ...
Mei-Feng Ruan   +9 more
core   +1 more source

Self‐Assembled Monolayers in p–i–n Perovskite Solar Cells: Molecular Design, Interfacial Engineering, and Machine Learning–Accelerated Material Discovery

open access: yesAdvanced Materials, EarlyView.
This review highlights the role of self‐assembled monolayers (SAMs) in perovskite solar cells, covering molecular engineering, multifunctional interface regulation, machine learning (ML) accelerated discovery, advanced device architectures, and pathways toward scalable fabrication and commercialization for high‐efficiency and stable single‐junction and
Asmat Ullah, Ying Luo, Stefaan De Wolf
wiley   +1 more source

Crystal structure of dimethyl 9H-carbazole-2,7-dicarboxylate

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2015
In the title compound, C16H13NO4, the carbazole ring system is almost planar with non-H atoms possessing a mean deviation from planarity of 0.037 Å. The two ester groups are orientated trans to one another and tilted slightly from the mean plane of the ...
Ryan L. Lehane   +3 more
doaj   +1 more source

Photoinduced copper-catalyzed C–N coupling with trifluoromethylated arenes

open access: yesNature Communications, 2023
Selective defluorinative functionalization of trifluoromethyl group (–CF3) is an attractive synthetic route to the pharmaceutically privileged fluorine-containing moiety. Herein, we report a strategy based on photoexcited copper catalysis to activate the
Jun Huang   +6 more
doaj   +1 more source

Synthesis of carbazoles, bis(carbazoles) and helicenes

open access: yes, 2022
RSEQ Symposium 2021.
Aragoncillo, Cristina   +2 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy