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Journal articles on the topic 'Tetraphenyl'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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1

Schwarz, Marián, Petr Trška, and Josef Kuthan. "NMR spectroscopic investigation of p-substituted 2,4,4,6-tetraphenyl-1,4-dihydropyridines and their oxa and thia analogues." Collection of Czechoslovak Chemical Communications 54, no. 7 (1989): 1854–69. http://dx.doi.org/10.1135/cccc19891854.

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The 1H, 13C and 19F NMR spectra of photochromic p-substituted 2,4,4,6-tetraphenyl-1,4-dihydropyridines IIa-IIg, 1-methyl-2,4,4,6-tetraphenyl-1,4-dihydropyridines IIIa-IIIg, 2,4,4,6-tetraphenyl-4H-pyrans IVa-IVh, and 2,4,4,6-tetraphenyl-4H-thiopyran V were inspected; it was found that compounds IIa-IIg occur in a dynamic equilibrium with their dihydro tautomer VIa-VIg. Also deuteriodeprotonation of IIa and IIIa and their reaction with trifluoroacetic acid were investigated by NMR spectroscopy.

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2

Schumann, Herbert, and Klaudia Sühring. "Di-, Hexa- und Deca-substituierte Decaphenylferrocene / Di-, Hexa- and Deca-Substituted Decaphenylferrocenes." Zeitschrift für Naturforschung B 60, no. 4 (2005): 383–88. http://dx.doi.org/10.1515/znb-2005-0404.

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5-Bromo-1,2,3,4-tetraphenyl-5-p-tolyl-1,3-cyclopentadiene (1a), 5-Bromo-1,4-di-phenyl-2,3,5- tri-p-tolyl-1,3-cyclopentadiene (1b), 5-Bromo-1,2,3,4,5-penta-p-tolyl-1,3-cyclopentadiene (1c), 5- Bromo-1,2,3,4-tetraphenyl-5-p-bromophenyl-1,3-cyclopentadiene (1d), and 5-Bromo-1,2,3,4-tetraphenyl- 5-p-anisyl-1,3-cyclopentadiene (1e) react with ironpentacarbonyl in m-xylene to yield the corresponding ferrocenes 2a - 2e. In the course of the purification procedure, reactions with HCl and the solvent m-xylene are observed which yield the mixed ionic sandwich complexes [(C5Ph4C6H4Me)Fe(C6H4Me2)]+Cl− (3a

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3

Chen, Tsu-yu Raymond, Mark R. Anderson, and Dennis G. Peters. "Electrochemistry of 1,1,4,4-tetraphenyl-1,3-butadiene, 1,1,4,4-tetraphenyl-1,2-butadiene, and 1,1,4,4-tetraphenyl-1-butene in dimethylformamide." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 197, no. 1-2 (1986): 341–58. http://dx.doi.org/10.1016/0022-0728(86)80159-0.

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4

Liu, Zishan, Liang Dong, Feifeng Li, Changjun Hou, Kun He, and Danqun Huo. "Determination of the binding mechanism of cobalt(II) meso-tetraphenyl porphyrin with plant-esterase." Polish Journal of Chemical Technology 23, no. 1 (2021): 25–30. http://dx.doi.org/10.2478/pjct-2021-0004.

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Abstract Plant-esterase (EC 3.1.1.X) has received much attention because plant esterase and acetylcholinesterase (AChE) share a similar sensitivity towards organophosphorus (OP) pesticides detection with the same inhibition mechanism. To improve the analytical performance, tetraphenyl metal porphyrin, as an indicator was introduced to combine with plant-esterase. The time of reach equilibrium in PBS solution was shortened after adding plant-esterase by assaying the intensify change of the porphyrin spectrum. Meanwhile, intensify of porphyrin spectrum with plant-esterase was increased compared

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5

Xie, Jin-Sheng, Xiao-Yun Hu, Zi-Xing Shan, and Zhong-Qiang Zhou. "A Straightforward and Practical Approach to Chiral Inducer: (2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenylbutane-2,3-diol." Australian Journal of Chemistry 68, no. 6 (2015): 995. http://dx.doi.org/10.1071/ch14505.

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A straightforward and practical access to chiral inducer (2R,3R)-1,4- dimethoxyl-1,1,4,4-tetraphenyl-2,3-diol has been developed. It is based on highly regioselective 2,3-cyclosulfitation of (2R,3R)-1,1,4,4-tetraphenyl-butanetetraol, in which selective protection of the secondary hydroxyls and chlorination of the tertiary hydroxyls of (2R,3R)-1,1,4,4-tetraphenyl-butanetetraol are accomplished via one step. In the preparation, methanol was used as a methylating reagent and common alkali liquor was used for cleavage of the protection group. It may be one of the most straightforward and practical

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6

Ogikubo, Junichi, Eileen Meehan, James T. Engle, Christopher J. Ziegler, and Christian Brückner. "Oxazolochlorins. 9.meso-Tetraphenyl-2-oxabacteriochlorins andmeso-Tetraphenyl-2,12/13-dioxabacteriochlorins." Journal of Organic Chemistry 78, no. 7 (2013): 2840–52. http://dx.doi.org/10.1021/jo400031r.

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7

Hanson, A. W., A. W. McCulloch, and A. G. McInnes. "Structural studies of 1,3-dioxa-2-silacycloalkanes." Canadian Journal of Chemistry 64, no. 7 (1986): 1400–1407. http://dx.doi.org/10.1139/v86-239.

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Crystal structure analyses of 1,3-dioxa-2,2-diphenyl-2-sila-5,6-benzocycloheptane (1), 2,9-disila-1,3,8,10-tetraoxa-2,2,9,9-tetraphenyl-5,6,12,13-dibenzocyclotetradecane (2), 2,10-disila-2,2,10,10-tetramethyl-1,3,9,11-tetraoxa-5,7,13,15-dibenzocyclohexadecane (3), 2,7-disila-2,2,7,7-tetramethyl-1,3,6,8-tetraoxa-4,5,9,10-dibenzocyclodecane (4), and 2,4-disila-2,2,4,4-tetraphenyl-1,3,5-trioxa-6,7-benzocycloheptane (11) are reported. Facile acid-catalyzed reaction of 2,7-disila-1,3,6,8-tetraoxa-2,2,7,7-tetraphenyl-4,5,9,10-dibenzocyclodecane (8) with water gives 1,3-di(2-hydroxyphenoxy)-1,3-disil

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8

He, Jiliang, and John F. Harrod. "Cyclization of Ph2Si(NHNHMe)2. II. Reactions with methyl iodide, HCl, and Ph2SiCl2, and thermolysis." Canadian Journal of Chemistry 72, no. 8 (1994): 1759–63. http://dx.doi.org/10.1139/v94-222.

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The reaction of Ph2Si(NHNHMe)2 (1) with MeI results in a mixture of two six-membered ring isomers, 1,2,4,5-tetraaza-1,4-dimethyl-3,3,6,6-tetraphenyl-3,6-disilacyclohexane (2), 45%, and 1,2,4,5-tetraaza-1,5-dimethyl-3,3,6,6-tetraphenyl-3,6-disilacyclohexane (3), 40%. The reaction of 1 with HCl or Ph2SiCl2 proceeds in a similar fashion. The thermolysis of 1 is studied from 25–600 °C. In the range of 250–300 °C, about 50% of 1 is converted into 2,3, and 1,2,4-triaza-1-methyl-4-methylamino-3,3,5,5-tetraphenyl-3,5-disilacyclopentane, 8. Possible pathways for the formation of 2,3, and 8 in these cyc

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9

Wang, Yanling, Qiang Peng, Ying Liang, Benlin Li, and Weiguo Zhu. "Theoretical Study of Optical and Electronic Properties of Unsymmetrical Dendritic Molecules with Different Bridge Moieties." Australian Journal of Chemistry 64, no. 11 (2011): 1475. http://dx.doi.org/10.1071/ch11114.

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Molecules bearing polyphenylphenyl dendrons show great potential for applications in organic light-emitting diodes. In this paper, quantum-chemical calculations have been applied to investigate the structural and electronic properties of typical molecules bearing polyphenylphenyl dendrons, 2-(2′,3′,4′,5′-tetraphenyl)phenyl-5-(p-N,N-dimethyl)phenyl pyridine (A), 1-(2′,3′,4′,5′-tetraphenyl)phenyl-4-(p-N,N-dimethyl)phenyl benzene (B), 2-(2′,3′,4′,5′-tetraphenyl)phenyl-5-(p-N,N-dimethyl)phenyl thiophene (C), 1-(2′,3′,4′,5′-tetraphenyl)phenyl-2,5-dimethoxy-4-(p-N,N-dimethyl)phenyl benzene (D), and

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10

Dueno, Eric E., Ricky Joseph Paul Gibson, Ralph Nicholas Salvatore, Robert D. Pike, and Cesar H. Zambrano. "2,2,3,3′-Tetraphenyl-7,7′-biquinoxaline." Acta Crystallographica Section E Structure Reports Online 64, no. 1 (2007): o110—o111. http://dx.doi.org/10.1107/s1600536807033521.

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11

Pourayoubi, Mehrdad, and Poorya Zargaran. "Tetraphenyl piperazine-1,4-diyldiphosphonate." Acta Crystallographica Section E Structure Reports Online 66, no. 12 (2010): o3273—o3274. http://dx.doi.org/10.1107/s1600536810047860.

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12

Zhao, Bing, Zhi-yu Li, Meng-jiao Fan, Bo Song, and Qi-gang Deng. "1,2,4,5-Tetraphenyl-1H-imidazole." Acta Crystallographica Section E Structure Reports Online 68, no. 2 (2012): o542. http://dx.doi.org/10.1107/s1600536812003145.

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13

Shimasaki, Choichiro, Yoshinori Muto, Nobuchika Takashima, Eiichi Tsukurimichi, Toshiaki Yoshimura, and Kiyoshi Hasegawa. "Pyrolysis of tetraphenyl imidodiphosphate." Journal of Analytical and Applied Pyrolysis 23, no. 3 (1992): 217–27. http://dx.doi.org/10.1016/0165-2370(92)80018-h.

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14

Bolag, Altan, and Yoshiro Yamashita. "Organic Field-Effect Transistors Based on 3’-Flouro-2,2',6,6'-Tetraphenyl-4,4'-Dipyranylidene." Solid State Phenomena 288 (March 2019): 37–43. http://dx.doi.org/10.4028/www.scientific.net/ssp.288.37.

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In this work, 3’-flouro-2,2',6,6'-tetraphenyl-4,4'-dipyranylidene (3FDP) was originally synthesized and investigated with density functional theory (DFT) calculations, ultraviolet–visible spectroscopy (UV–Vis) and cyclic voltammetry (CV) in comparison with 2,2',6,6'-tetraphenyl-4,4'-dipyranylidene (DP) and 4’-flouro-2,2',6,6'-tetraphenyl-4,4'-dipyranylidene (4FDP). 3FDP-based organic field-effect transistors (OFETs) were fabricated with bottom contact configuration on bare SiO2/Si substrate, 1,1,1,3,3,3-hexamethyldisilazane (HMDS) and octadecyltrichlorosilane (OTS) treated substrate, respectiv

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15

Mori, Y., and K. Maeda. "2,4,4,6-Tetraphenyl-3(4H)-pyridinone." Acta Crystallographica Section C Crystal Structure Communications 47, no. 12 (1991): 2682–83. http://dx.doi.org/10.1107/s0108270191007485.

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16

Rachlewicz, Krystyna, Natasza Sprutta, Piotr J. Chmielewski, and Lechosław Latos-Grażyński. "Characterisation of new 26,28-diheterosapphyrins: 5,10,15,20-tetraphenyl-26,28-dioxasapphyrin and 5,10,15,20-tetraphenyl-26,28-dithiasapphyrin." Journal of the Chemical Society, Perkin Transactions 2, no. 4 (1998): 969–76. http://dx.doi.org/10.1039/a705496c.

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17

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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18

Chou, Dei Wei, Kan Lin Chen, Chien Jung Huang, et al. "Enhanced Brightness and Efficiency in Single-Layer White Polymer Light-Emitting Diodes (PLEDs)." Key Engineering Materials 434-435 (March 2010): 429–33. http://dx.doi.org/10.4028/www.scientific.net/kem.434-435.429.

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In this paper, the improvements in luminance and efficiency have been demonstrated in a white polymer light-emitting device (PLED) with the structure of ITO/ poly (N-vinylcarbazole) (PVK): 1,1,4,4- tetraphenyl-1,3-butadiene (TPB):5,6,11,12-tetrapheny lanpthacene (rubrene) /LiF(1 nm)/Ca(10 nm)/Al(100 nm). The luminance of the white PLED is up to 4940 cd/m2 at 17 V. The current efficiency and Commission Internationale d’Eclairage (CIE) coordinates is 1.66 cd/A and (0.325, 0.326), respectively. The enhancement of the luminance and efficiency can be attributed to an improved hole-injection ability

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19

Sun, Hongmei, Kai Guo, Haifeng Gan, Xin Li, and Christopher A. Hunter. "Influence of receptor flexibility on intramolecular H-bonding interactions." Organic & Biomolecular Chemistry 13, no. 29 (2015): 8053–66. http://dx.doi.org/10.1039/c5ob00805k.

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20

Pollard, Travis P., and Thomas L. Beck. "Re-examining the tetraphenyl-arsonium/tetraphenyl-borate (TATB) hypothesis for single-ion solvation free energies." Journal of Chemical Physics 148, no. 22 (2018): 222830. http://dx.doi.org/10.1063/1.5024209.

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21

Zhang, Yuyang, Huifang Li, Gaobin Zhang та ін. "Aggregation-induced emission enhancement and mechanofluorochromic properties of α-cyanostilbene functionalized tetraphenyl imidazole derivatives". Journal of Materials Chemistry C 4, № 14 (2016): 2971–78. http://dx.doi.org/10.1039/c5tc03348a.

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22

Rautela, Ranjana, Neeraj K. Joshi, Sacha Novakovic, et al. "Determinants of the efficiency of photon upconversion by triplet–triplet annihilation in the solid state: zinc porphyrin derivatives in PVA." Physical Chemistry Chemical Physics 19, no. 34 (2017): 23471–82. http://dx.doi.org/10.1039/c7cp04746k.

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23

Beil, Sebastian B., Sabine Möhle, Patrick Enders, and Siegfried R. Waldvogel. "Electrochemical instability of highly fluorinated tetraphenyl borates and syntheses of their respective biphenyls." Chemical Communications 54, no. 48 (2018): 6128–31. http://dx.doi.org/10.1039/c8cc02996b.

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24

Zamborlini, Giovanni, Matteo Jugovac, Albano Cossaro, et al. "On-surface nickel porphyrin mimics the reactive center of an enzyme cofactor." Chemical Communications 54, no. 95 (2018): 13423–26. http://dx.doi.org/10.1039/c8cc06739b.

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25

Ning, Di, Qiao Liu, Qian Wang, Xiao-Meng Du, Yue Li, and Wen-Juan Ruan. "Pyrene-based MOFs as fluorescent sensors for PAHs: an energetic pathway of the backbone structure effect on response." Dalton Transactions 48, no. 17 (2019): 5705–12. http://dx.doi.org/10.1039/c9dt00492k.

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26

Souza, P., M. A. Mendiola, A. Arquero, V. Fernández, E. Gutiérrez-Puebla, and C. Ruiz-Valero. "Copper(II) Complexes of Hydrazone Derivatives." Zeitschrift für Naturforschung B 49, no. 2 (1994): 263–71. http://dx.doi.org/10.1515/znb-1994-0219.

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Three benzil based, macrocyclic oxygen-, nitrogen-, and sulfur-containing ligands, (3,4,10,11 -tetraphenyl-1,2,5,6,8,9,12,13-octaazacyclotetradeca-7,14-dithione-2,4,9,11 -tetraene) ethanol (L1), 10,1 l-diethoxy-3,4,10,11-tetraphenyl-1,2,5,6,8,9,12,13-octaazacyclotetradeca- 7.14-dithione-2,4-diene (L2), (3,4,10,11 -tetraphenyl-1,2,5,6,8,9,12,13-octaazacyclotetradeca- 7.14-dione-2,4,9,l 1-tetraene) ethanol (L3); a cyclic ligand, 6-ethoxy-l,6-diphenyl-4-oxo- 3,4,5,6-tetrahydro-2,3,5-triazine (L5) and two open chain ligands, benzilsemicarbazone (L6) and benzilbisthiosemicarbazone (L4) are reported

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27

Bai, Ling, Zhiqiang Zheng, Zhongqiang Wang, Feng He, Yurui Xue, and Ning Wang. "Acetylenic bond-driven efficient hydrogen production of a graphdiyne based catalyst." Materials Chemistry Frontiers 5, no. 5 (2021): 2247–54. http://dx.doi.org/10.1039/d1qm00064k.

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28

Markin, Andrei, Ali K. Ismael, Ross J. Davidson, et al. "Conductance Behavior of Tetraphenyl-Aza-BODIPYs." Journal of Physical Chemistry C 124, no. 12 (2020): 6479–85. http://dx.doi.org/10.1021/acs.jpcc.9b10232.

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29

Sun, Xiaoqiang, Liang Chen, Yan Jiang, and Zhengyi Li. "3,3,9,9-Tetraphenyl-2,4,8,10-tetraoxaspiro[5.5]undecane." Acta Crystallographica Section E Structure Reports Online 66, no. 11 (2010): o3035. http://dx.doi.org/10.1107/s1600536810043795.

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30

Schwarz, Marián, and Josef Kuthan. "Alkylation of 2,4,4,6-tetraphenyl-1,4-dihydropyridine." Collection of Czechoslovak Chemical Communications 54, no. 7 (1989): 1870–79. http://dx.doi.org/10.1135/cccc19891870.

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A series of photochromic N-methyl derivatives IIIa-IIIh was synthesized by alkylation of 1-sodio-2,4,4,6-tetraphenyl-1,4-dihydropyridine (II) in an inert atmosphere. On the other hand, the starting material II afforded products IVa and IVb in the presence of atmospheric oxygen. Mechanisms of acidobasic transformations of compounds IVa and IVb are discussed and spectral characteristics of new compounds are interpreted.

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31

Aluri, Bhaskar R., Stephan Peitz, Anina Wöhl та ін. "1,1,2,2-Tetraphenyl-1λ5-diphosphane 1-sulfide". Acta Crystallographica Section E Structure Reports Online 65, № 2 (2009): o404. http://dx.doi.org/10.1107/s1600536809002955.

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32

Bolte, M. "1,1-Dichloro-3,3,5,5-tetraphenyl-1λ4,2,6,3λ5,5λ5-selenadiazadiphosphorin". Acta Crystallographica Section C Crystal Structure Communications 51, № 6 (1995): 1209–11. http://dx.doi.org/10.1107/s0108270194008334.

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33

Llorca, J., E. Molins, A. Flores-Vela, S. Cruz-Sánchez, and E. Juaristi. "4,6,10,12-Tetraphenyl-7,9-dioxa-1,3-dithiacyclododecane." Acta Crystallographica Section C Crystal Structure Communications 53, no. 6 (1997): 816–18. http://dx.doi.org/10.1107/s0108270197000759.

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34

Schmidbaur, Hubert, Christos Paschalidis, Oliver Steigelmann та Gerhard Müller. "5-Methyl-1,1,3,3-tetraphenyl-1λ5,3λ5-diphosphabenzol". Angewandte Chemie 102, № 5 (1990): 569–71. http://dx.doi.org/10.1002/ange.19901020523.

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35

Beintema, J., P. Terpstra, and W. J. van Weerden. "The Crystallography of Pentaerythrol Tetraphenyl Ether." Recueil des Travaux Chimiques des Pays-Bas 54, no. 8 (2010): 627–30. http://dx.doi.org/10.1002/recl.19350540808.

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36

Subha Nandhini, M., R. V. Krishnakumar, T. Narasimhamurthy, V. Vijayakumar, M. Sundaravadivelu, and S. Natarajan. "4,8,9,10-Tetraphenyl-1,3-diazaadamantan-6-one." Acta Crystallographica Section E Structure Reports Online 58, no. 6 (2002): o675—o677. http://dx.doi.org/10.1107/s1600536802008772.

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37

Vojtěchovský, J., and J. Hašek. "Structure of 2,4,4,6-tetraphenyl-4H-pyran." Acta Crystallographica Section C Crystal Structure Communications 46, no. 9 (1990): 1727–30. http://dx.doi.org/10.1107/s010827019000049x.

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38

Clark, George R., Deborah M. Tonei, Warren R. Roper, and L. James Wright. "3,3,6,6-Tetraphenyl-trans-tricyclo[3.1.0.02,4]hexane." Acta Crystallographica Section E Structure Reports Online 62, no. 2 (2006): o534—o535. http://dx.doi.org/10.1107/s1600536806000092.

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39

Svarovskaya, N. V., N. S. Kobotaeva, and E. E. Sirotkina. "Redox behavior of metal tetraphenyl porphins." Russian Journal of Electrochemistry 36, no. 8 (2000): 829–32. http://dx.doi.org/10.1007/bf02757054.

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40

Moghimi, Abolghasem, Mehdi Ghandi, Sedigheh Sadat Naeemi, Nasser Safari, and Farzad Bahadoran. "Benzo-9-crown-3 substituted phenyl porphyrin." Journal of Porphyrins and Phthalocyanines 11, no. 09 (2007): 676–81. http://dx.doi.org/10.1142/s1088424607000771.

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41

Johnson, MD, CA Mcintosh та VC Reinsborough. "Binding of Nitrogen Heterocyclic Ligands and Tetraphenyl-Substituted Ions by β-Cyclodextrins". Australian Journal of Chemistry 47, № 1 (1994): 187. http://dx.doi.org/10.1071/ch9940187.

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Binding constants obtained spectrofluorometrically are reported for β- cyclodextrin (substituted and unsubstituted ) inclusion of several commonly used nitrogen heterocyclic ligands and tetraphenyl-substituted ions.

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42

Wang, Shun, Yuchuan Liu, Yu Ye, et al. "Ultrahigh volatile iodine capture by conjugated microporous polymer based on N,N,N′,N′-tetraphenyl-1,4-phenylenediamine." Polymer Chemistry 10, no. 20 (2019): 2608–15. http://dx.doi.org/10.1039/c9py00288j.

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43

Zhou, Xiang, Manli Huang, Xuan Zeng, et al. "Combining the qualities of carbazole and tetraphenyl silane in a desirable main chain for thermally activated delayed fluorescence polymers." Polymer Chemistry 10, no. 30 (2019): 4201–8. http://dx.doi.org/10.1039/c9py00742c.

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44

Ryan, P. T. P., P. L. Lalaguna, F. Haag, et al. "Validation of the inverted adsorption structure for free-base tetraphenyl porphyrin on Cu(111)." Chemical Communications 56, no. 25 (2020): 3681–84. http://dx.doi.org/10.1039/c9cc09638h.

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45

Li, Xiao-Dong, Hua-Ping Zang, Jun-Tao Wang, Jun-Fei Wang, and Hong Zhang. "Design of tetraphenyl silsesquioxane based covalent-organic frameworks as hydrogen storage materials." J. Mater. Chem. A 2, no. 43 (2014): 18554–61. http://dx.doi.org/10.1039/c4ta02692f.

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46

Strohmann, Carsten, and Eric Wack. "Bis-, Tris- and Tetrakis(lithiomethyl)germanes: New Building Blocks for Organogermanium Compounds." Zeitschrift für Naturforschung B 59, no. 11-12 (2004): 1570–78. http://dx.doi.org/10.1515/znb-2004-11-1230.

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Bis(lithiomethyl)germanes, R2Ge(CH2Li)2, tris(lithiomethyl)germanes, RGe(CH2Li)3, and tetrakis( lithiomethyl)germane, Ge(CH2Li)4, were prepared by the reductive C-S bond cleavage with lithium naphthalenide (LiC10H8) or lithium p,p’-di-tert-butylbiphenylide (LiDBB) and characterized by trapping with Bu3SnCl. The bis(lithiomethyl)germanes were used for the synthesis of 1,1-dimethyl-3,3-diphenyl-1-germa-3-silacyclobutane, 1,1-diethyl-3,3-diphenyl-1-germa-3-silacyclobutane, 1,1,3,3-tetraphenyl-1-germa-3-silacyclobutane and 1,1,3,3-tetraphenyl-1,3-digermacyclobutane. The single-crystal X-ray diffra

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Raimondo, Luisa, Silvia Trabattoni, and Adele Sassella. "Control of post-growth processes for the selection of metallo-tetraphenylporphyrin nanowires." Physical Chemistry Chemical Physics 21, no. 16 (2019): 8482–88. http://dx.doi.org/10.1039/c8cp07747a.

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Lee, Jiwon, Yoona Park, Joori Jung, and Won-Sik Han. "Blue-shifted aggregation-induced emission of siloles by simple structural modification and their application as nitro explosive chemosensors." Photochem. Photobiol. Sci. 16, no. 10 (2017): 1495–501. http://dx.doi.org/10.1039/c7pp00268h.

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By substituting methyl groups at ortho positions of peripheral tetraphenyl rings on the silacyclopentadiene ring, intramolecular rotations were successfully controlled and the photophysical properties were varied.

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EL-Mahdy, Ahmed F. M., Mohamed Gamal Mohamed, Tharwat Hassan Mansoure, Hsiao-Hua Yu, Tao Chen, and Shiao-Wei Kuo. "Ultrastable tetraphenyl-p-phenylenediamine-based covalent organic frameworks as platforms for high-performance electrochemical supercapacitors." Chemical Communications 55, no. 99 (2019): 14890–93. http://dx.doi.org/10.1039/c9cc08107k.

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In this study we synthesized two tetraphenyl-p-phenylenediamine-based covalent organic frameworks (TPPDA-TPPyr and TPPDA-TPTPE COFs) for potential use in high-performance electrochemical supercapacitors.

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Tomaszewski, Patryk, Marcin Wiszniewski, Janusz Serwatowski, Krzysztof Woźniak, Krzysztof Durka, and Sergiusz Luliński. "Synthesis of tetraarylborates via tetralithio intermediates and the effect of polar functional groups and cations on their crystal structures." Dalton Transactions 47, no. 46 (2018): 16627–37. http://dx.doi.org/10.1039/c8dt04068k.

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