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Thematische Bibliographien / Diphenyl carbazone / Zeitschriftenartikel

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Zeitschriftenartikel zum Thema „Diphenyl carbazone“

Autor: Grafiati

Veröffentlicht am 18. Mai 2024

Zuletzt aktualisiert am 26. Juli 2025

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1

Maniasso, Nelson, and Elias A. G. Zagatto. "Flow-injection spectrophotometric catalytic determination of manganese in plants exploiting the aerial oxidation of diphenyl carbazone." Analytica Chimica Acta 366, no. 1-3 (1998): 87–92. http://dx.doi.org/10.1016/s0003-2670(97)00682-x.

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2

Kalogirou, Andreas S., and Panayiotis A. Koutentis. "5,5′-Bis[9-(2-ethylhexyl)-9H-carbazol-3-yl]-4,4′-diphenyl-2,2′-bithiazole." Molbank 2024, no. 1 (2024): M1761. http://dx.doi.org/10.3390/m1761.

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Stille coupling between 5,5′-dibromo-4,4′-diphenyl-2,2′-bithiazole and 9-(2-ethylhexyl)-3-(tributylstannyl)-9H-carbazole in the presence of Pd(Ph3P)2Cl2 in toluene, heated at reflux for 2 h, gave 5,5′-bis[9-(2-ethylhexyl)-9H-carbazol-3-yl]-4,4′-diphenyl-2,2′-bithiazole in 85% yield.

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3

Zhang, Zunting, Yang Kang, Rong Hou, Xiaoyan Min, Tao Wang, and Yong Liang. "An Oxidant- and Catalyst-Free Synthesis of Dibenzo[a,c]carbazoles via UV Light Irradiation of 2,3-Diphenyl-1H-indoles." Synthesis 54, no. 06 (2021): 1621–32. http://dx.doi.org/10.1055/a-1677-4881.

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AbstractAn efficient methodology for the synthesis of dibenzo[a,c]carbazoles via annulation of 2,3-diphenyl-1H-indoles in EtOH under UV light irradiation (λ = 365 nm) along with hydrogen evolution is described. This method exhibits the advantages of mild reaction conditions, no requirement of any oxidants and catalysts, and release of hydrogen as the only byproduct. Notably, the mechanism investigation confirms that the trans-4b,8a-dihydro-9H-dibenzo[a,c]carbazole intermediate could convert into cis-4b,8a-dihydro-9H-dibenzo[a,c]carbazole, which relies on the nitrogen atom of the indole ring. T

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4

Vyas, Tanmay, and Abhijeet Joshi. "Carbon Quantum Dots (CQDs)-Diphenyl Carbazone (DPCO) loaded thin film sensors for fluorescent and colorimetric dual mode detection of mercury in various water resources." Optical Materials 154 (August 2024): 115700. http://dx.doi.org/10.1016/j.optmat.2024.115700.

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5

Çiçek, Baki, Merve Çağlı, Remziye Tülek, and Ali Teke. "Synthesis and optical characterization of bipod carbazole derivatives." Heterocyclic Communications 26, no. 1 (2020): 148–56. http://dx.doi.org/10.1515/hc-2020-0111.

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AbstractIn this study, some new biscarbazole derivatives were synthesized for the purpose of being used in OLED technologies and related areas. The following compounds: {1,2-bis(2-(3,6-diphenyl-9H-carbazole-9-yl) ethoxy)ethane (C-1), bis[2-(2-(3,6- diphenyl-9H-carbazole-9-yl) ethoxy)etyl]ether (C-2), bis[2-(2-(3,6-di(naphthalene-1-yl)-9H-carbazol-9-yl)ethoxy)etyl]ether (C-3) and bis [2-(2-(3,6-di(naphthalene-2-yl)-9H-carbazol-9-yl)ethoxy) ethyl]ether (C-4) were synthesized by Suzuki-Miyaura Cross Coupling reactions. The structural properties of the synthesized compounds were characterized by F

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6

Guo, Huixia, Xiaohua Xi, Renxiang Yan та Xiaoquan Lu. "Theoretical study on the effect of different π-linker on the performance of sensitizer in carbazole-based dyes". Journal of Theoretical and Computational Chemistry 17, № 02 (2018): 1850019. http://dx.doi.org/10.1142/s0219633618500190.

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Derived from diarylamine sensitizer diphenyl-(7-pyridin-4-yl-9H-carbazol-2-yl)-amine (N13), a series of novel D[Formula: see text]A carbazole-based organic dye sensitizers with different [Formula: see text]-linkers were designed for searching more effective sensitizers in dye-sensitized solar cells (DSSCs) design. Optimized geometries, electronic structure, and other parameters, which can evaluate the performance of DSSCs effectively and intuitively, were theoretically calculated by density functional theory (DFT) and time-dependent DFT methods at the M06/6-31G(d,p) level. The results indicate

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Xiao, Zhanhai, Yi Di, Zhifang Tan, Xudong Cheng, Bing Chen, and Jiwen Feng. "Efficient organic dyes based on perpendicular 6,12-diphenyl substituted indolo[3,2-b]carbazole donor." Photochemical & Photobiological Sciences 15, no. 12 (2016): 1514–23. http://dx.doi.org/10.1039/c6pp00286b.

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Three novel indolo[3,2-b]carbazole-based dyes have been designed and synthesized using a 6,12-diphenyl substituted indolo[3,2-b]carbazole as a donor, a thiophene cyanoacrylic acid moiety as electron acceptor and anchoring group, together with triphenylamine, 3,4,5-trimethoxybenzene and bromine as a second donor.

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8

Zhang, Zhaohang, Wei Jiang, Xinxin Ban, et al. "Solution-processed efficient deep-blue fluorescent organic light-emitting diodes based on novel 9,10-diphenyl-anthracene derivatives." RSC Advances 5, no. 38 (2015): 29708–17. http://dx.doi.org/10.1039/c5ra00627a.

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9

Mekuskiene, Giedrute, Sigitas Tumkevicius, and Povilas Vainilavicius. "5-(4,6-Diphenyl-2-pyrimidinyl)-1,3,4-oxa(thia)diazoles and 1,2,4-triazoles." Journal of Chemical Research 2002, no. 5 (2002): 213–15. http://dx.doi.org/10.3184/030823402103171898.

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Synthesis of 5-(4,6-diphenyl-2-pyrimidinyl)-1,3,4-oxa(thia)diazoles and corresponding 1,2,4-triazoles from 4,6-diphenyl-2-pyrimidinecarboxylic acid hydrazide and 1-(4,6-diphenyl-2-pyrimidinylcarbonyl)-4-phenylthiosemi-carbazide is described.

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10

Liu, Bei, Zheng Chen, Liming Lin, Yuntao Han, Jinhui Pang, and Zhenhua Jiang. "Synthesis and characterization of poly(arylene ether ketone)s with 3,6-diphenyl-9H-carbazole pendants using C–N coupling reaction." High Performance Polymers 29, no. 5 (2016): 575–84. http://dx.doi.org/10.1177/0954008316655592.

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3,6-Diphenyl-9 H-carbazole pendants are grafted herein to poly(arylene ether ketone)s (PAEKs) via the Ullmann C–N coupling reaction. To the best of our knowledge, this is the first time that PAEKs containing a carbazole pendant (Cz) have been synthesized through the Ullmann C–N coupling reaction. The high molecular weights of PAEK-Cz (PAEKs with 3,6-diphenyl-9 H-carbazole pendants) are inherited from their precursors, owing to the high reactivity of their monomers. The obtained PAEK-Cz- x polymers exhibit good solubility in most common organic solvents and excellent thermal stabilities, with t

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11

Warmiati, Warmiati, and Wijayanti Wijayanti. "Reaction Stability Test of Hexavalent Chromium Complex with 1,5-Diphenylcarbazide in Analysis using UV Visible Spectrophotometer." Indonesian Journal of Chemical Research 11, no. 3 (2024): 218–22. http://dx.doi.org/10.30598/ijcr.2024.11-war.

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A reaction stability test of hexavalent chromium complex with 1,5-diphenyl carbazide in analysis using a UV Visible Spectrophotometer has been done in this study. This study aims to find out the colored complex stability for the reaction of chromium hexavalent and diphenyl carbazide in the analysis of hexavalent chromium using a UV Vis spectrophotometer in terms of time. The sample was measured in 540 nm of wavelength with 10, 30, 60, 90, 120, and 180-minute time intervals. Each interval was carried out with two times replications. There were no significant differences in the colored complex u

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12

Dhar, Abhishek, Nadavala Siva Kumar, Mohammad Asif та Rohit L. Vekariya. "Fabrication of D–π–A sensitizers based on different donors substituted with a dihydropyrrolo[3,4-c]pyrrole-1,4-dione bridge for DSSCs: influence of the CDCA co-absorbent". New Journal of Chemistry 42, № 14 (2018): 12024–31. http://dx.doi.org/10.1039/c8nj00847g.

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The effect of co-absorbance on the performance of DSSC devices with a new design of dimer sensitizers possessing a 2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione (DPP) bridge and various donor groups (carbazole, diphenyl amine, indole) are reported in the present work.

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13

Muneer, Mohammed, Prashant V. Kamat, and Manapurathu V. George. "Electron transfer reactions. Reaction of nitrogen heterocycles with potassium." Canadian Journal of Chemistry 68, no. 6 (1990): 969–75. http://dx.doi.org/10.1139/v90-152.

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The results of our studies on potassium-induced transformations of some selected nitrogen heterocycles are presented. The substrates under investigation include 2,3-diphenylindole (1a), 2,3-diphenyl-1-methylindole (1b), 1,2,3-triphenylindole (1c), 2,3,4,5-tetraphenylpyrrole (5a), 1,2,3,5-tetraphenylpyrrole (5b), 1-benzyl-2,3,5-triphenylpyrrole (5c), 2,4,5-triphenyloxazole (15a), 4,5-diphenyl-2-methyloxazole (15b), 2,4-diphenyl-5-methyloxazole (15c), and 2,4,5-triphenylimidazole (19). Treatment of 1a with potassium in THF gave 9H-dibenzo[a,c]carbazole (3a), whereas 1c gave a mixture of 9-phenyl

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LEE, SEUNG EUN, HYUN NAM CHO, SUNG HYUN JUNG, HO CHEOL PARK, CHANG JUNE LEE, and JONG WOOK PARK. "NOVEL SYNTHESIS OF HIGHLY PHENYL-SUBSTITUTED SPIROBIFLUORENE AND CARBAZOLE DERIVATIVES THROUGH DIELS–ALDER REACTION FOR LIGHT-EMITTING DIODES." Journal of Nonlinear Optical Physics & Materials 14, no. 04 (2005): 469–74. http://dx.doi.org/10.1142/s0218863505002906.

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We synthesized and characterized novel highly phenyl-substituted spirobifluorene and carbazole derivatives such as 3,6-bis[(2,3,4,5-tetraphenyl)phenyl]-9-ethylcarbazole (BTPEC); 3,6-bis(7,10-diphenyl-fluoranthene)-9-ethylcarbazole (BDFEC); 2,7-Bis[(2,3,4,5-tetraphenyl)phenyl]-9,9′-spirobifluorene (BTPSF); and 3,6-bis(7,10-diphenyl-fluo-ran-thene)-9,9′-spirobifluorene (BDFSF), through Diels–Alder reaction. BDFEC showed sky blue PL spectrum at 481 nm and BTPSF showed ultra-violet PL spectrum at 374 nm in chloroform solution. Also BTPEC and BDFSF exhibited PL spectrum at around the UV region, 390

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15

Gümrükçüoğlu, Nurhan, and Bahar Bilgin Sökmen. "Synthesis of oxadiazole substituted new carbazole derivatives as antioxidant and antiurease agent." European Journal of Biological Research 12, no. 2 (2022): 181–89. https://doi.org/10.5281/zenodo.6612440.

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Heterocyclic compounds containing nitrogen together with an oxygen atom in their structures are an important class of medicinal chemistry compounds due to their interesting diverse biological applications. Some compounds including carbazole ring, which are aromatic organic compounds in tricyclic structure, show biological activity in a wide spectrum. Oxadiazole compounds attract the attention of many chemists thanks to their antibacterial, antitumor, anticancer, anti-viral, antimicrobial, anti-HIV, antituberculosis and antioxidant properties. In this study, new oxadiazole substituted carbazole

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16

Bezvikonnyi, Oleksandr, Ronit Sebastine Bernard, Viktorija Andruleviciene, et al. "Derivatives of Imidazole and Carbazole as Bifunctional Materials for Organic Light-Emitting Diodes." Materials 15, no. 23 (2022): 8495. http://dx.doi.org/10.3390/ma15238495.

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New derivatives of carbazole and diphenyl imidazole for potential multiple applications were synthesized and investigated. Their properties were studied by thermal, optical, photophysical, electrochemical, and photoelectrical measurements. The compounds exhibited relatively narrow blue light-emission bands, which is favorable for deep-blue electroluminescent devices. The synthesized derivatives of imidazole and carbazole were tested as fluorescent emitters for OLEDs. The device showed deep-blue emissions with CIE color coordinates of (0.16, 0.08) and maximum quantum efficiency of 1.1%. The com

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17

El-Kabbany, F., S. Talia, A. Shehap, and M. M. El-Naggar. "THERMOPLASTIC PHENOMENON IN REHEATED DIPHENYL CARBAZIDE C13H14N4O." Journal of Physics and Chemistry of Solids 59, no. 9 (1998): 1619–25. http://dx.doi.org/10.1016/s0022-3697(98)00060-2.

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18

El-Kabbany, F., S. Taha, A. Shehap, and M. M. El-Naggar. "Infrared spectroscopic characterization of aluminized diphenyl carbazide." Infrared Physics & Technology 40, no. 4 (1999): 295–303. http://dx.doi.org/10.1016/s1350-4495(99)00002-x.

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19

Lim, Eunhee. "Synthesis and Characterization of Carbazole-Benzothiadiazole-Based Conjugated Polymers for Organic Photovoltaic Cells with Triazole in the Main Chain." International Journal of Photoenergy 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/607826.

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We have synthesized a series of carbazole-benzothiadiazole-triazole based copolymers, poly[(N-9′-heptadecanyl-2,7-carbazole)-co-(5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole))-co-((4-(4-butylphenyl)-3,5-diphenyl-4H-1,2,4]triazole))] (PCz3TBTz) by Suzuki coupling polymerization. The optical and electrochemical properties of the copolymers could be tuned by changing the comonomer unit of triazole from 0% to 80%. Organic photovoltaic (OPV) cells were fabricated by blending the synthesized polymers as a donor and PCBM as an acceptor. The material solubility and film morphology were improved b

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20

Aminah, Nanik S., Tin M. Thant, Alfinda N. Kristanti, Rico Ramadhan, Hnin T. Aung та Yoshiaki Takaya. "Carbazomarin: A New Potential of α-Glucosidase Inhibitor From Clausena excavata Roots". Natural Product Communications 14, № 12 (2019): 1934578X1989407. http://dx.doi.org/10.1177/1934578x19894076.

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Continuing our exploration for dual functions antidiabetic and antioxidant agents from Myanmar medicinal plant , a new carbazole-pyranocoumarin conjugate, carbazomarin-C (1) along with a known carbazole alkaloid, mukonine (2) and a pyranocoumarin, xanthoxyletin (3), was isolated from the roots of Clausena excavata. The chemical structures of these compounds were identified using a combination of spectroscopic methods. Among isolates, there was a strong inhibition of compounds (1) and (3) on yeast α-glucosidase in a dose-dependent manner. It was shown when p-nitrophenyl-α-d-glucopyranoside was

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Jo, Seunghyeon, Sangwook Park, Hyukmin Kwon, Hayoon Lee, Kiho Lee, and Jongwook Park. "Synthesis and Electrical Properties of a New Bipolar Material Using Spacer Moiety." Applied Sciences 14, no. 9 (2024): 3593. http://dx.doi.org/10.3390/app14093593.

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To develop a deep-blue emitter, a molecule with bipolar characteristics was designed as a donor-spacer-acceptor type, in which 9-(4-(4,6-diphenyl-1),3,5-triazin-2-yl)-2,5-dimethylphenyl)-9H-carbazole (DTPCZ)—with carbazole as an electron donating group and a diphenyl triazine moiety as an electron accepting group—was successfully synthesized. The photoluminescence (PL) maxima of DTPCZ were 421 nm in the solution state and 425 nm in the film state, indicating emission in the deep-blue region. DTPCZ also exhibited high thermal stability, with a degradation temperature of 349 °C. To confirm the e

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Shao, Pin, Zhen Li, Jingui Qin, Hongmei Gong, Sha Ding, and Ququan Wang. "New Heterocycle-Based Organic Molecule with Two-Photon Induced Blue Fluorescent Emission." Australian Journal of Chemistry 59, no. 1 (2006): 49. http://dx.doi.org/10.1071/ch05179.

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A new heterocycle-based quadrupolar molecule containing 2,5-diphenyl-1,3,4-oxadiazole as the π-centre and two carbazoles as end units has been synthesized. It exhibits two-photon induced blue emission, and its two-photon absorption cross section in the femtosecond region is measured to be 239 × 10−50 cm4 s photon−1 at a wavelength of 788 nm.

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Huang, Bin, Wei Jiang, Yuan Yuan Liu, et al. "Thermally Activated Delayed Fluorescence Materials Based on Carbazole/Sulfone." Advanced Materials Research 1044-1045 (October 2014): 158–63. http://dx.doi.org/10.4028/www.scientific.net/amr.1044-1045.158.

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A series of bipolar materials for thermally activated delayed fluorescence (TADF) based on carbazole and diphenylsulfone, is synthesized by Ulmann and Suzuki coupling reactions. In these materials, the 3,6-di-tert-butylcarbazole and N-phenylcarbazole group as donors are linked at the 3-, 4-position of diphenyl sulfone. The electronic, photophysical and electrochemical properties of these materials are studied by extensive UV-vis, fluorescence spectroscopic measurements, cyclic voltammetry as well as theoretical calculations. The energy gap between singlet and triplet (△EST) in these materials

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Hafez, Marwa, S. El-Sayed, and S. A. Sayed. "Spectroscopic Properties and Micro-Structure for Promising Solar Cell Application of Ruthenium-Diphenyl Carbazide (RuDPC) Complex." Key Engineering Materials 921 (May 30, 2022): 129–44. http://dx.doi.org/10.4028/p-xuf3fq.

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The variation in the modes of a new ruthenium diphenyl carbazide complex (RuDPC) during changing of ruthenium (Ru) concentration within 0.01 ≤ X ≤ 0.09 in diphenyl carbazide (DPC) are investigated using IR analysis. Variation in some IR spectroscopic parameters during the increase of Ru content in pure DPC has been recorded. The variation in both the relaxation time and the rotational energy barrier for RuDPC samples at the mode 505 cm-1 supports a change that occurs at X ≈ 0.05. Micro-structure of RuDPC samples was studied by X-ray analysis and scanning electron microscopy. Moreover, SEM pict

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Bhasikuttan, A. C., D. K. Palit, A. V. Sapre, and J. P. Mittal. "Photophysical characteristics of diphenyl carbazide-laser flash photolysis and fluorescence studies." Chemical Physics Letters 316, no. 1-2 (2000): 67–74. http://dx.doi.org/10.1016/s0009-2614(99)01204-x.

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A. Hamdoon, Enam. "Indirect Spectrophotometric Determination of Mesalazine via Chromate-1,5-Diphenyl carbazide Complex." Rafidain Journal of Science 27, no. 2 (2018): 69–78. http://dx.doi.org/10.33899/rjs.2018.145392.

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Yamazoe, Atsushi, Osami Yagi, and Hiroshi Oyaizu. "Biotransformation of fluorene, diphenyl ether, dibenzo-p-dioxin and carbazole by Janibacter sp." Biotechnology Letters 26, no. 6 (2004): 479–86. http://dx.doi.org/10.1023/b:bile.0000019554.49484.40.

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Silva Wakabayashi, Priscila Sayoko, Rodrigo da Costa Duarte, Luís Gustavo Teixeira Alves Duarte, et al. "Synthesis and thermal, electrochemical, and photophysical investigation of carbazole/diphenyl benzothiadiazole-based fluorophores." Dyes and Pigments 182 (November 2020): 108668. http://dx.doi.org/10.1016/j.dyepig.2020.108668.

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El-Kabbany, F., S. Taha, F. M. Mansey, and A. Shehap. "Infrared study for the phase transition of re-heated diphenyl carbazide C13H14N4O." Infrared Physics & Technology 38, no. 3 (1997): 169–75. http://dx.doi.org/10.1016/s1350-4495(97)00004-2.

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Shahroosvand, Hashem, Leyla Heydari, Sara Tarighi, Mohammadreza Riahi, Babak Nemati Bideh, and Babak Pashaei. "Aqueous dye-sensitized solar cell based on new ruthenium diphenyl carbazide complexes." International Journal of Hydrogen Energy 42, no. 26 (2017): 16421–27. http://dx.doi.org/10.1016/j.ijhydene.2017.04.222.

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Tang, Huaijun, Zhiguo Zhang, Changjie Cong та Keli Zhang. "Synthesis of a novel β-diketone containing carbazole and 2,5-diphenyl-1,3,4-oxadiazole fragments". Russian Journal of Organic Chemistry 45, № 4 (2009): 559–63. http://dx.doi.org/10.1134/s1070428009040150.

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Park, Sunwoo, Hyukmin Kwon, Sangwook Park, et al. "New Bipolar Host Materials Based on Indolocarbazole for Red Phosphorescent OLEDs." Materials 17, no. 17 (2024): 4347. http://dx.doi.org/10.3390/ma17174347.

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We designed and synthesized new indolocarbazole-triazine derivatives, 9-di-tert-butyl-5,7-bis(4-(4,6-diphenyl-1,3,5-triazin-2-yl)phenyl)-5,7-dihydroindolo[2,3-b]carbazole (2TRZ-P-ICz) and 3,9-di-tert-butyl-5,7-bis(5′-(4,6-diphenyl-1,3,5-triazin-2-yl)-[1,1′:3′,1″-terphenyl]-2′-yl)-5,7-dihydroindolo[2,3-b]carbazole (2TRZ-TP-ICz), as new bipolar host materials for red phosphorescent OLEDs. In the film state, 2TRZ-P-ICz and 2TRZ-TP-ICz exhibited photoluminescence maxima at 480 nm and 488 nm, respectively. The dipole moment characteristics of the new compounds under various solvent conditions were

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Krupashankar, D. S., and M. Shakthi Rathna. "Absence of Chromates in Detergents in India Confirmed by Diphenyl Carbazide Spot Test." Dermatitis 20, no. 6 (2009): 351–52. http://dx.doi.org/10.2310/6620.2009.09033.

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El-Kabbany, F., S. Taha, and M. Hafez. "A kinetic investigation and X-ray analysis of thermal shrinkage of diphenyl carbazide." Thermochimica Acta 510, no. 1-2 (2010): 122–25. http://dx.doi.org/10.1016/j.tca.2010.07.005.

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El-Kabbany, F., S. Taha, M. Hafez, and N. R. Abdel Aziz. "Infrared study and phase transformation of the new lithium–diphenyl carbazide complex (LiDPC)." Journal of Molecular Structure 1092 (July 2015): 113–21. http://dx.doi.org/10.1016/j.molstruc.2015.03.015.

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Borse, Tushar H., Vijay L. Maheshwari, and Manisha P. Baviskar. "Effect of Diphenyl Carbazide on the Metribuzin Induced Inhibition of Photosystem-II Photochemistry." Journal of Plant Biochemistry and Biotechnology 9, no. 2 (2000): 119–21. http://dx.doi.org/10.1007/bf03263097.

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Kondagorla, Shivshankar R., and Swapnil V. Madhamshettiwar. "Adsorption of Chromium (VI) from Wastewater Using Blended Natural Adsorbent." Oriental Journal Of Chemistry 40, no. 4 (2024): 1134–37. http://dx.doi.org/10.13005/ojc/400427.

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In this study adsorption of chromium (VI) ion by using blended natural novel adsorbent like neem leaves powder with peanut shell powder. The batch Adsorption experiments were conducted by different proportions of blended neem leaf powder and peanut shells powder and variations in the weight of adsorbents, contact time at room temperature, and various pH. Investigate the concentration of adsorbate before adsorption and after adsorption by 1, 5 Diphenyl Carbazide Colorimetric method with reference to calibration curve. Results obtained by blended neem leaves powder with peanut shell powder adsor

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Liu, Gang, Der-Jang Liaw, Wei-Yi Lee, et al. "Tristable electrical conductivity switching in a polyfluorene–diphenylpyridine copolymer with pendant carbazole groups." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 367, no. 1905 (2009): 4203–14. http://dx.doi.org/10.1098/rsta.2008.0262.

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Tristable electrical conductivity switching and non-volatile memory effects are demonstrated in a conjugated copolymer of poly(2,6-diphenyl-4-((9-ethyl)-9 H -carbazole)-pyridinyl- alt -2,7-(9,9-didodecyl)-9 H -fluorenyl) (PPCzPF). The indium–tin oxide (ITO)/PPCzPF/Al device can be switched from the low-conductivity (off) state to the first high-conductivity (on-1) state at 1.8 V, with an on/off current ratio of approximately 100. The device can be further switched from the on-1 state to the next higher conductivity (on-2) state at 2.4 V, with an on-2/on-1 current ratio of approximately 20. All

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Rassi, Salwa Fares. "Preparation and Charactreization Selective Electrode for Determination of CopperIon(II)." Journal of Electrochemical Science and Engineering 5, no. 4 (2016): 237. http://dx.doi.org/10.5599/jese.236.

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<span>Achemically modified carbon paste electrode with diphenyl carbazide the potentiometric determination of Cu(II) is demonstrated. The electrode exhibits linear response to Cu(II) over a wide concentration range (9.2×10−7-5.0×10−1) with Nernstian slope of 30±0.15 mV per decade. It has a response time of about 40 s and can be used for a period of two months with good reproducibility. The detection limit of this electrode was 7.0×10−7 M. The proposed electrode shows a very good selectivity for Cu(II) over a wide variety of metal ions. This chemically modified carbon paste electrode was

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Zommere, Margarita Anna, Natalija Tetervenoka, Anna Pidluzhna, et al. "Original Blue Light-Emitting Diphenyl Sulfone Derivatives as Potential TADF Emitters for OLEDs." Coatings 14, no. 10 (2024): 1294. http://dx.doi.org/10.3390/coatings14101294.

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Organic light-emitting diodes (OLEDs) have emerged as one of the dominant technologies in displays due to their high emission efficiency and low power consumption. However, the development of blue color emitters has fallen behind that of red and green emitters, posing challenges in achieving optimal efficiency, stability, and accessibility. In this context, thermally activated delayed fluorescence (TADF) emitters hold promise as a potential solution for cost-effective, exceptionally efficient, and stable blue OLEDs due to their potential high efficiency and stability. TADF is a principle where

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Kremser, Gabriele, Oliver T. Hofmann, Stefan Sax, et al. "Synthesis and Photophysical Properties of 3,6-Diphenyl-9-hexyl-9H-carbazole Derivatives Bearing Electron Withdrawing Groups." Monatshefte für Chemie - Chemical Monthly 139, no. 3 (2008): 223–31. http://dx.doi.org/10.1007/s00706-007-0774-3.

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Zheng, Yanan, Jinnan Huo, Shu Xiao, Heping Shi, Dongge Ma, and Ben Zhong Tang. "Synthesis, photoluminescence and electroluminescence properties of a new blue emitter containing carbazole, acridine and diphenyl sulfone units." Organic Electronics 101 (February 2022): 106411. http://dx.doi.org/10.1016/j.orgel.2021.106411.

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Chang, Yufei, Yuliang Wu, Kaiyuan Zhang, et al. "1,8-diphenyl-carbazole-based boron, sulfur-containing multi-resonance emitters with suppressed aggregation emission for narrowband OLEDs." Dyes and Pigments 220 (December 2023): 111678. http://dx.doi.org/10.1016/j.dyepig.2023.111678.

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Brendle, James J., Abram Outlaw, Arvind Kumar, et al. "Antileishmanial Activities of Several Classes of Aromatic Dications." Antimicrobial Agents and Chemotherapy 46, no. 3 (2002): 797–807. http://dx.doi.org/10.1128/aac.46.3.797-807.2002.

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ABSTRACT Aromatic dicationic molecules possess impressive activity against a broad spectrum of microbial pathogens, including Pneumocystis carinii, Cryptosporidium parvum, and Candida albicans. In this work, 58 aromatic cations were examined for inhibitory activity against axenic amastigote-like Leishmania donovani parasites. In general, the most potent of the compounds were substituted diphenyl furan and thiophene dications. 2,5-Bis-(4-amidinophenyl)thiophene was the most active compound. This agent displayed a 50% inhibitory concentration (IC50) of 0.42 ± 0.08 μM against L. donovani and an i

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El-Kabbany, F., S. Taha, and M. Hafez. "A study of the phase transition of reheated diphenyl carbazide (DPC) by using UV spectroscopy." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 128 (July 2014): 481–88. http://dx.doi.org/10.1016/j.saa.2014.02.143.

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Sivakumar, K., T. Stalin, and N. Rajendiran. "Dual fluorescence of diphenyl carbazide and benzanilide: Effect of solvents and pH on electronic spectra." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 62, no. 4-5 (2005): 991–99. http://dx.doi.org/10.1016/j.saa.2005.04.033.

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Sutanu, Maiti, Neogi Sudarsan, and K. Dutta Binay. "Mechanism and kinetics of reduction of Cr(VI) by D-glucose in aqueous phase." Journal of Indian Chemical Society Vol. 96, Apr 2019 (2019): 557–61. https://doi.org/10.5281/zenodo.5638139.

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School of Environmental Science and Engineering, Department of Chemical Engineering, Indian Institute of Technology, Kharagpur-721 302, West Bengal, India. <em>E-mail</em>: bkdutta@iitkgp.ac.in <em>Manuscript received online 12 February 2019, accepted 14 March 2019</em> Among the various reducing agents used for remediation of Cr(VI) in contaminated soil, glucose is an attractive one since it has reasonable cost and does not have any adverse effect when an excess is used to satisfy the process needs. The objective of this work was to investigate the process of reduction and the kinetics and me

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Studzinsky, S. L. "Photoconductive, photovoltaic and information properties of new carbazole-based oligomeric film compositions doped with 2,2-diphenyl-1-picrylhydrazyl." Molecular Crystals and Liquid Crystals 639, no. 1 (2016): 126–36. http://dx.doi.org/10.1080/15421406.2016.1255043.

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Gajghate, D. G., E. R. Saxena, and A. L. Aggarwal. "Removal of chromium (VI) as chromium diphenyl carbazide (CDC) complex from aqueous solution by activated carbon." Water, Air, & Soil Pollution 65, no. 3-4 (1992): 329–37. http://dx.doi.org/10.1007/bf00479896.

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SUN Jun, 孙军, 张玉祥 ZHANG Yu-xiang, 赵卫华 ZHAO Wei-hua, 张宏科 ZHANG Hong-ke, 何海晓 HE Hai-xiao, and 田密 TIAN Mi. "Highly Efficient Red Electrophosphorescent Devices Based on 7-(9H-carbazol-9-yl)-N,N-diphenyl-9,9′-spirobi［fluoren］-2-amine Host Material." Chinese Journal of Luminescence 35, no. 3 (2014): 327–31. http://dx.doi.org/10.3788/fgxb20143503.0327.

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