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Antimicrobial Potential of Carbazole Derivatives [PDF]

open access: yes, 2022
Amongst many nitrogen-containing heterocycles, carbazole frame is the building block of various biologically active compounds, including both synthetic and natural products of which its antimicrobial and antifungal activities are the most examined.
Kadnor, Vijay A.
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

Advancements in Carbazole-Based Sensitizers and Hole-Transport Materials for Enhanced Photovoltaic Performance

open access: yesMolecules
Carbazole-based molecules play a significant role in dye-sensitized solar cells (DSSCs) due to their advantageous properties. Carbazole derivatives are known for their thermal stability, high hole-transport capability, electron-rich (p-type ...
Ayagoz Ibrayeva   +5 more
doaj   +1 more source

Ethyl 2-(1,2,3,4-tetrahydrospiro[carbazole-3,2′-[1,3]dioxolan]-9-yl)acetate

open access: yesActa Crystallographica Section E, 2009
In the title compound, C18H21NO4, the hydrogenated six-membered ring of the carbazole unit adopts a half-chair conformation. The dioxolane ring and ethylacetate substituent point to opposite sides of the carbazole plane.
Philipp M. G. Löffler   +2 more
doaj   +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

Recent Progress in the Isolation and Bioactivities of Carbazole Alkaloids

open access: yesNatural Product Communications
Objective/Background Carbazole derivatives have a tricyclic skeleton, consisting of a central pyrrole ring fused with two benzene rings. Carbazole derivatives are an important class of nitrogen-containing heterocyclic compounds that are widely found in ...
Duc Dau-Xuan   +2 more
doaj   +1 more source

Synthesis of Novel Derivatives of Carbazole-Thiophene, Their Electronic Properties, and Computational Studies

open access: yesJournal of Chemistry, 2016
A series of carbazole-thiophene dimers, P1–P9, were synthesized using Suzuki-Miyaura and Ullmann coupling reactions. In P1–P9, carbazole-thiophenes were linked at the N-9 position for different core groups via biphenyl, dimethylbiphenyl, and phenyl ...
E. F. Damit   +3 more
doaj   +1 more source

1-[6-(9H-Carbazol-9-yl)hexyl]-2-phenyl-1H-benzimidazole

open access: yesActa Crystallographica Section E, 2009
The molecule of the title compound, C31H29N3, contains a hexyl chain, a coordination unit (benzimidazole) and a functional group (carbazole). The benzimidazole ring is not coplanar with either the phenyl ring or the carbazole system, making dihedral ...
Jing Meng, Tian-Zhi Yu, Yu-Ling Zhao
doaj   +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

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