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Relevant bibliographies by topics / Tetraphenylmethane derivatives

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Journal articles

Academic literature on the topic 'Tetraphenylmethane derivatives'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Tetraphenylmethane derivatives"

1

Laliberté, Dominic, Thierry Maris, and James D. Wuest. "Molecular tectonics Use of urethanes and ureas derived from tetraphenylmethane and tetraphenylsilane to build porous chiral hydrogen-bonded networks." Canadian Journal of Chemistry 82, no. 2 (2004): 386–98. http://dx.doi.org/10.1139/v03-208.

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Tetraphenylmethane, tetraphenylsilane, and simple derivatives with substituents that do not engage in hydrogen bonding typically crystallize as close-packed structures with essentially no space available for the inclusion of guests. In contrast, derivatives with hydrogen-bonding groups are known to favor the formation of open networks that include significant amounts of guests. To explore this phenomenon, we synthesized six new derivatives 5a5e and 6a of tetraphenylmethane and tetraphenylsilane with urethane and urea groups at the para positions, crystallized the compounds, and determined the

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2

Fournier, Jean-Hugues, Xin Wang, and James D. Wuest. "Derivatives of tetraphenylmethane and tetraphenylsilane: Synthesis of new tetrahedral building blocks for molecular construction." Canadian Journal of Chemistry 81, no. 5 (2003): 376–80. http://dx.doi.org/10.1139/v03-056.

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Useful derivatives of tetraphenylmethane and tetraphenylsilane have been synthesized by efficient methods that give crystalline products without chromatographic purification. New compounds include tetrakis(4-hydroxyphenyl)methane (21), tetrakis(4-formylphenyl)methane (22), tetrakis[(4-hydroxymethyl)phenyl]methane (23), tetrakis(4-bromophenyl)silane (24), tetrakis(4-iodophenyl)silane (25), tetrakis(4-hydroxyphenyl)silane (26), tetrakis[(4-hydroxymethyl)phenyl]silane (27), and tetrakis[(4-chloromethyl)phenyl]silane (28). These compounds are valuable precursors for the construction of complex mol

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3

Basavoju, Srinivas, Srinivasulu Aitipamula, and Gautam R. Desiraju. "Host–guest and network structures of some tetraphenylmethane derivatives." CrystEngComm 6, no. 25 (2004): 120–25. http://dx.doi.org/10.1039/b403858b.

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4

Enzmann, Armin, and Wolfgang Beck. "Metal Complexes of Biologically Important Ligands, CLV [1]. Some Derivatives of 4-Ethynylphenylalanine." Zeitschrift für Naturforschung B 59, no. 8 (2004): 865–68. http://dx.doi.org/10.1515/znb-2004-0817.

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AbstractThe benzoyl protected 4-ethynyl-L-phenylalanine methyl ester gives with octacarbonyldicobalt and ethylene-bis(triphenylphosphine)platinum(0) the complexes Co2(CO)6(HC≡CR) and (Ph3P)2 Pt(HC≡CR) (R = p-C6H4CH2CH(CO2Me)N(HCOPh). The heterocumulene [Cp(Ph3P)2Ru=C=C(H)R]+BF4− (R = p-C6H4CH2C(H)N(H)-Boc is formed from [Cp(Ph3P)2Ru]+BF4− and N-t-Boc-4-ethynylphenylalanine methyl ester. The alkynyl bridged tetraamino acid with a tetraphenylmethane backbone C[p-C6H4C≡C-p-C6H4-CH2CH(CO2Me)NH-t- Boc]4 was synthesized from tetrakis(4-iodophenyl)methane and N-Boc-4-ethynylphenylalanine methyl ester

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5

Shu, Haiyang, Hua Li, Jiancheng Rao, et al. "Room-temperature phosphorescence from a purely organic tetraphenylmethane derivative with formyl groups in both solution and crystalline states." Journal of Materials Chemistry C 8, no. 41 (2020): 14360–64. http://dx.doi.org/10.1039/d0tc04070c.

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A tetraphenylmethane derivative with four aldehyde groups (TPM-4CHO) exhibits clear blue phosphorescence in common organic solvents at room temperature. Additionally, bright green phosphorescence can be observed in its crystal.

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6

Perez, Olivier, Clarisse Bloyet, Jean-Michel Rueff, et al. "Topochemical Route from Supramolecular to Hybrid Materials: Tetraphenylmethane-Based Tectons and Lanthanum Phosphonate Derivative." Crystal Growth & Design 16, no. 12 (2016): 6781–89. http://dx.doi.org/10.1021/acs.cgd.6b00823.

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7

Kotha, Sambasivarao, and Manoranjan Behera. "Preparation of Functionalized Tetraphenylmethane Derivatives via the Suzuki-Miyaura Cross-Coupling Reaction." ChemInform 38, no. 14 (2007). http://dx.doi.org/10.1002/chin.200714107.

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8

Liu, Chuan-Zhi, Jingjing Wang, Bo Yang, et al. "Two and Three-Dimensional Halogen-Bonded Frameworks: Self-assembly Influenced by Crystallization Solvents." Chemical Communications, 2023. http://dx.doi.org/10.1039/d3cc02981f.

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In this paper, two types of solid phase 2D and 3D XBOFs were selectively constructed from identical building blocks of tetraphenylmethane tetrapyridine derivative and 1,4-diiodotetrafluorobenzene by changing the crystallization solvent....

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9

Chen, Chin-Ti, Tzu-Yao J. Lin, Hsiu-Chih Yeh, Li-Hsin Jan, Easwaramoorthy Balasubramaniam, and Yu-Tai Tao. "Tetraphenylmethane-Based 1,3,4-Oxadiazole as Electron Transporting Materials in Organic Light-Emitting Devices." MRS Proceedings 598 (1999). http://dx.doi.org/10.1557/proc-598-bb3.5.

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ABSTRACTA series of tetrahedral tetramers of 2,5-diphenyl substituted 1,3,4-oxadiazole compounds were synthesized and characterized for electron-transporting layer (ETL) in organic light-emitting diode (OLED). The multiple-branch design of the oxadiazole tetramers intends to increase the melting temperature and to generate glass phase of the low molar mass derivative such as 2-(4-biphenylyl)-5-(4-tert-butylphenyl)-1,3,4-oxadiazole (PBD). We observed temperatures of the glass phase transition for the oxadiazole tetramer with appropriate peripheral substituents, indicative of amorphous character

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