Artykuły w czasopismach na temat „N-phenyl”

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1

Ajibade, Peter A., Benjamin C. Ejelonu i Bernard Omondi. "N-Ethyl-N-phenyl{[ethyl(phenyl)carbamothioyl]disulfanyl}carbothioamide". Acta Crystallographica Section E Structure Reports Online 68, nr 7 (23.06.2012): o2182. http://dx.doi.org/10.1107/s1600536812027808.

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2

Shen, Heng-Shui, Nan Liu, Zi-Cheng Li i Wen-Cai Huang. "N-Ethyl-N-phenyl-N′-tosylformamidine". Acta Crystallographica Section E Structure Reports Online 65, nr 7 (17.06.2009): o1582. http://dx.doi.org/10.1107/s1600536809021953.

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3

Fu, T. Y., J. R. Scheffer i J. Trotter. "N-Phenyl-N-(phenylthioxomethyl)benzamide". Acta Crystallographica Section C Crystal Structure Communications 54, nr 1 (15.01.1998): 101–2. http://dx.doi.org/10.1107/s0108270197011244.

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4

Dou, Shi-qi, B. Thimme Gowda, Helmut Paulus i Alarich Weiss. "The Bond N-Cl. Crystal Structures and 35Cl NQR of N-Chloro-N-Phenyl-2-chloroacetamide, N-Chloro-N-phenyl-2,2-dichloroacetamide, N-Chloro-N-phenyl-2,2,2-trichloroacetamide, and N-Phenyl-2,2,2-trichloroacetamide". Zeitschrift für Naturforschung A 49, nr 12 (1.12.1994): 1136–44. http://dx.doi.org/10.1515/zna-1994-1206.

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Abstract The crystal structures of C6H5NClCOCH2Cl (1), C6H5NClCOCHCl2 (2), C6H5NClCOCCl3 (3),and C6H5NHCOCCl3 (4) have been determined at room temperature (lattice constants, d in pm).(1): P21 /c, Z = 4, a = 738, b = 645, c = 1891, β = 90.41°, d (N -C l) = 171, d (C = O ) = 121; (2): P21 /c, Z = 4, a = 820, b = 1495, c = 905, β = 114.78°, d (N -Cl) = 171, d (C = O ) = 120; (3): P 21/c, Z = 4,a = 819, b = 1853, c = 718, β = 103.64°, d (N -Cl) = 172, d (C = O ) = 120; (4): P21/c, Z = 4, a = 551, b = 1704, c = 1035, β = 93.08°, d (C = O) = 121.For (2), (3), and (4) the 35Cl NQR frequencies have been determined in the range 77 ≤ T /K ≤ 300. At 77 K (γ in MHz): (2): γ(w,1) = 37.600, γ(w,2) = 38.188, γ(N) = 51.858; (3): γ(w,1) = 39.944, γ(w,2) = 40.512, γ(w,3) = 40.739, γ(N) = 52.791; (4): γ(w,1) = 39.428, γ(w,2) = 39.452, γ(w,3) = 39.986. For the compound C6H5NHCOCHCl2 (5) the 35Cl NQ R measured at 77 K is: γ(w,1) = 37.195 MHz, γ(w,2) = 37.596 MHz. The relation, γ(35Cl) = d (N -Cl) is discussed.
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5

Han, Li-Ping, Bin Li, Jie Liu i Qing-Chun Liu. "N-Phenyl-N-{4-[5-(2-phenyl-3-pyridyl)-1,3,4-oxadiazol-2-yl]phenyl}aniline". Acta Crystallographica Section E Structure Reports Online 63, nr 12 (21.11.2007): o4780. http://dx.doi.org/10.1107/s1600536807058382.

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6

Young Chang, Ji, Tae Ja Kim, Man Jung Han i Kyu Ho Chae. "Polymerization of N-[4-(azidocarbonyl)phenyl]maleimide and N-[4-(N′-phenoxycarbonylamino)phenyl]maleimide". Polymer 40, nr 14 (czerwiec 1999): 4049–54. http://dx.doi.org/10.1016/s0032-3861(98)00600-4.

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7

Özçelik, Suzan, Muharrem Dinçer, Memet Şekerci, Ayla Balaban i Ümmühan Özdemir. "N-Phenyl-N′-(2-thienylmethylene)hydrazine". Acta Crystallographica Section E Structure Reports Online 60, nr 9 (21.08.2004): o1552—o1553. http://dx.doi.org/10.1107/s1600536804019932.

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8

Fu, T. Y., J. R. Scheffer i J. Trotter. "N-Phenyl-N-(phenylthioxomethyl)benzamide. Erratum". Acta Crystallographica Section C Crystal Structure Communications 54, nr 4 (15.04.1998): 562. http://dx.doi.org/10.1107/s0108270198003357.

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9

Mo, Shanyan. "N-Cyano-N-phenyl-p-toluenesulfonamide". Synlett 25, nr 09 (11.04.2014): 1337–38. http://dx.doi.org/10.1055/s-0033-1341246.

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10

Khan, Islam Ullah, Mehmet Akkurt, Faiza Anwar i Shahzad Sharif. "N-[4-(N-Cyclohexylsulfamoyl)phenyl]acetamide". Acta Crystallographica Section E Structure Reports Online 66, nr 4 (20.03.2010): o868—o869. http://dx.doi.org/10.1107/s160053681000961x.

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11

Khan, Islam Ullah, Zeeshan Haider, Muhammad Nadeem Arshad i Sharafat Ali. "N-Ethyl-N-phenyl-p-toluenesulfonamide". Acta Crystallographica Section E Structure Reports Online 66, nr 4 (31.03.2010): o979. http://dx.doi.org/10.1107/s1600536810011219.

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12

Hoque, Md Ehtesham Ul, i Hai-Whang Lee. "Pyridinolysis of Phenyl N-Phenyl Phosphoramidochloridate in Acetonitrile". Bulletin of the Korean Chemical Society 33, nr 10 (20.10.2012): 3437–40. http://dx.doi.org/10.5012/bkcs.2012.33.10.3437.

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13

PARKIN, JUDITH, NICK P. TOMKINSON i RICHARD VIRDEN. "Inhibition of chymotrypsin by phenyl N-phenyl-phosphoramidochloridate". Biochemical Society Transactions 20, nr 3 (1.08.1992): 283S. http://dx.doi.org/10.1042/bst020283s.

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14

Datta, Mritunjoy, Alan J. Buglass i Mark R. J. Elsegood. "N-Phenyl-tert-butanesulfinamide". Acta Crystallographica Section E Structure Reports Online 65, nr 8 (29.07.2009): o2034. http://dx.doi.org/10.1107/s1600536809028633.

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15

Yu, Da-sheng, Fang-shi Li, Wei Yao, Yin-hong Liu i Chui Lu. "N,N-Dimethyl-N′-[3-(trifluoromethyl)phenyl]urea". Acta Crystallographica Section E Structure Reports Online 64, nr 7 (7.06.2008): o1220. http://dx.doi.org/10.1107/s1600536808016656.

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16

Capella, Laura, Antonella Capperucci, Giovanni Curotto, Dario Lazzari, Pasquale Dembech, Gianna Reginato i Alfredo Ricci. "Silylcupration of N-phenyl-N-ethynyl-aniline: A versatile route to functionalized N,N-bis(phenyl)enamines". Tetrahedron Letters 34, nr 20 (maj 1993): 3311–14. http://dx.doi.org/10.1016/s0040-4039(00)73691-4.

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17

Ajibade, Peter A., i Damian C. Onwudiwe. "Synthesis and characterization of group 12 complexes of N,N-methyl phenyl-N,N-butyl phenyl dithiocarbamate". Journal of Coordination Chemistry 64, nr 17 (19.08.2011): 2963–73. http://dx.doi.org/10.1080/00958972.2011.606906.

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18

Gataullin, Rail R., Ivan S. Afon’kin, Akhnaf A. Fatykhov, Leonid V. Spirikhin i Il’dus B. Abdrakhmanov. "Iodocyclization of N-(2-nitrophenyl)- and N-phenyl-N’-[2-(alk-1-enyl)phenyl]ethanimidamides". Mendeleev Communications 11, nr 5 (styczeń 2001): 201–2. http://dx.doi.org/10.1070/mc2001v011n05abeh001490.

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19

Kühnau, Hans-Hellmut, i Horst-Robert Schütte. "Synthesen radioaktiv markierter Verbindungen; Synthese von N-Phenyl-N'-dimethylharnstoff(Fenuron)-[Phenyl-14C] und N-Phenyl-N'-dimethylharnstoff(Fenuron)-[14CH3] bzw. N-(p-Chlorphenyl)-N'-dimethylharnstoff(Monuron-[14CH3]". Zeitschrift für Chemie 9, nr 6 (1.09.2010): 231–32. http://dx.doi.org/10.1002/zfch.19690090609.

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20

Han, Li-Ping, Bin Li i Jie Liu. "N-Phenyl-N-{4-[5-(4-pyridyl)-1,3,4-oxadiazol-2-yl]phenyl}aniline". Acta Crystallographica Section E Structure Reports Online 64, nr 1 (12.12.2007): o242. http://dx.doi.org/10.1107/s1600536807065245.

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21

Wang, Zhi-Qiang, Rui Zhang, Xiao-Juan Sun, Ya-Peng Zhang, Yan Xu i Chen Xu. "Crystal structure of N-phenyl-N-(4-(pyren-1- yl)phenyl)benzenamine, C34H23N". Zeitschrift für Kristallographie - New Crystal Structures 225, nr 3 (wrzesień 2010): 573–74. http://dx.doi.org/10.1524/ncrs.2010.0251.

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22

Chopra, Deepak, A. R. Choudhury, K. Nagarajan i T. N. Guru Row. "N-Phenylethyl-N'-[3-(trifluoromethyl)phenyl]thiourea". Acta Crystallographica Section E Structure Reports Online 60, nr 11 (9.10.2004): o1970—o1971. http://dx.doi.org/10.1107/s1600536804024961.

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23

Manjare, Sudesh T., Ray J. Butcher i Harkesh B. Singh. "N-[2-(2-Bromobenzylamino)phenyl]-N-butylformamide". Acta Crystallographica Section E Structure Reports Online 65, nr 11 (23.10.2009): o2826. http://dx.doi.org/10.1107/s1600536809042883.

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24

Pavia, Michael R., Sandra J. Lobbestael, Charles P. Taylor, Fred M. Hershenson i David L. Miskell. "N-Phenyl-N'-pyridinylureas as anticonvulsant agents". Journal of Medicinal Chemistry 33, nr 2 (luty 1990): 854–61. http://dx.doi.org/10.1021/jm00164a061.

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25

Fun, Hoong-Kun, Chin Wei Ooi, Dinesha, S. Viveka i G. K. Nagaraja. "(Z)-N-[2-(N′-Hydroxycarbamimidoyl)phenyl]acetamide". Acta Crystallographica Section E Structure Reports Online 69, nr 3 (9.02.2013): o370—o371. http://dx.doi.org/10.1107/s1600536813003371.

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26

Podkopaeva, O. Y., D. L. Kuznetsov, V. D. Belov i Y. V. Chizhov. "Electronic structure of phenyl-N,N-dimorpholinomethanes". Journal of Structural Chemistry 41, nr 4 (lipiec 2000): 616–25. http://dx.doi.org/10.1007/bf02683924.

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27

CAPELLA, L., A. CAPPERUCCI, G. CUROTTO, D. LAZZARI, P. DEMBECH, G. REGINATO i A. RICCI. "ChemInform Abstract: Silylcupration of N-Phenyl-N-ethynylaniline: A Versatile Route to Functionalized N,N-Bis(phenyl)enamines." ChemInform 24, nr 41 (20.08.2010): no. http://dx.doi.org/10.1002/chin.199341145.

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28

Shadab, Mohd, i Mohammad Aslam. "Synthesis and Characterization of Some Transition Metal complexes with N-phenyl-N’-[substituted phenyl] Thiourea". Material Science Research India 11, nr 1 (30.08.2014): 83–89. http://dx.doi.org/10.13005/msri/110111.

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A series of thiourea ligand , N-N'- diphenyl thiourea [I] [DPTH], N-phenyl-N'-[2-phenoyl] thiourea [II] [PPTH], N-phenyl-N'-[2-chlorophenyl] thiourea III [PCPTH], N-phenyl-N'- [5-chloro-2-methyl phenyl] thiourea IV [PCMPTH] and N- phenyl -N'-(5-chloro-2-methoxy phenyl) thiourea V (PCMTPTH) and their transition metal complexes of the type ML2 and ML2 Cl2 have been synthesized by reacting phenyl isothiocyanate with substituted aniline and transition metal salts. These newly synthesized ligands and their complexes were characterized by elemental and spectral studies. Based upon these studies it was revealed that in all the cases metal is coordinated through suphur group of thioamide of ligands. In case of nickel complexes, the nickel is coordinated to both oxygen and sulphur. In all the complexes metal is tetra coordinated forming a square planer geometry.
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29

Dikic, Branko, Stephen G. Pyne, Brian W. Skelton i Allan H. White. "(2 R *, S S *)- N -Phenyl- N -(2-N′- Tert -Butyldiphenylsilyl- S -Phenylsulfonimidoyl-1-Phenyl)Ethylamine". Sulfur Letters 25, nr 2 (1.01.2002): 63–66. http://dx.doi.org/10.1080/02786110211432.

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30

Albores-Velasco, Martha, John Thorne i Ralph L. Wain. "Fungicidal activity of phenyl N-(4-substituted-phenyl)thionocarbamates." Journal of Agricultural and Food Chemistry 43, nr 8 (sierpień 1995): 2260–61. http://dx.doi.org/10.1021/jf00056a054.

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31

Fortin, Sébastien, Emmanuel Moreau, Jacques Lacroix, Jean-Claude Teulade, Alexandre Patenaude i René C-Gaudreault. "N-Phenyl-N′-(2-chloroethyl)urea analogues of combretastatin A-4: Is the N-phenyl-N′-(2-chloroethyl)urea pharmacophore mimicking the trimethoxy phenyl moiety?" Bioorganic & Medicinal Chemistry Letters 17, nr 7 (kwiecień 2007): 2000–2004. http://dx.doi.org/10.1016/j.bmcl.2007.01.023.

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32

Percino, Teresa Mancilla, Roxana Magaly Flores Ancona i Marisol López Martínez. "New strategy to the synthesis of (N→B) phenyl[N-alkyliminodiacetate-O,O′,N]boranes: The crystal structure of (N→B) phenyl[N-benzyliminodiacetate-O,O′,N]borane, (N→B)phenyl[N-(4-methyl)benzyliminodiacetate-O,O′,N]borane and (N→B) phenyl[N-phenacyliminodiacetate-O,O′,N]borane". Polyhedron 28, nr 13 (wrzesień 2009): 2771–75. http://dx.doi.org/10.1016/j.poly.2009.05.043.

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33

Muruganandam, L., S. Rajeswari, D. Tamilvendan, V. Ramkumar i G. Venkatesa Prabhu. "N-[Morpholino(phenyl)methyl]benzamide". Acta Crystallographica Section E Structure Reports Online 65, nr 3 (21.02.2009): o578. http://dx.doi.org/10.1107/s1600536809005327.

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34

Yin, Guodong, Shengli Hu, Yitao Li i Anxin Wu. "N-[4-(Phenylethynyl)phenyl]benzamide". Acta Crystallographica Section E Structure Reports Online 61, nr 8 (16.07.2005): o2561—o2562. http://dx.doi.org/10.1107/s1600536805022105.

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35

Chin, Taylor, Frank R. Fronczek i Ralph Isovitsch. "N-[4-(Morpholinodiazenyl)phenyl]acetamide". Acta Crystallographica Section E Structure Reports Online 65, nr 12 (25.11.2009): o3206. http://dx.doi.org/10.1107/s160053680904937x.

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36

Sun, Xiaofei, Xiaoping Zhang, Binbin Zhang, Wenguo Wang i Qingle Zeng. "(S)-N-Phenyl-tert-butanesulfinamide". Acta Crystallographica Section E Structure Reports Online 68, nr 6 (16.05.2012): o1728. http://dx.doi.org/10.1107/s1600536812020673.

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The asymmetric unit of the title compound, C10H15NOS, contains two independent molecules with similar conformations. In the crystal, molecules are linked in a head-to-tail fashion by N—H...O hydrogen bonds into chains running along the b axis. The absolute configuration was assigned on the basis of known chirality of the parent compound.
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37

Rehman, Jeveria, Ejaz, Islam Ullah Khan, William T. A. Harrison i Sidra Farid. "N-[4-(Ethylsulfamoyl)phenyl]acetamide". Acta Crystallographica Section E Structure Reports Online 67, nr 9 (27.08.2011): o2455. http://dx.doi.org/10.1107/s1600536811033472.

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38

Ahmad, Saba, Muhammad Akhyar Farrukh, Fahim Ashraf Qureshi, Islam Ullah Khan i Mehmet Akkurt. "N-[4-(Propylsulfamoyl)phenyl]acetamide". Acta Crystallographica Section E Structure Reports Online 68, nr 2 (7.01.2012): o290—o291. http://dx.doi.org/10.1107/s1600536811055528.

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39

John, Peter, Waqar Ahmad, Islam Ullah Khan, Shahzad Sharif i Edward R. T. Tiekink. "N-[4-(Benzylsulfamoyl)phenyl]acetamide". Acta Crystallographica Section E Structure Reports Online 66, nr 8 (17.07.2010): o2048. http://dx.doi.org/10.1107/s1600536810027698.

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40

Zhang, Wen-Jie, Jian-Xin Chen, Zhong-Shui Li, Ai-Ke Li i Xin-Rong Lin. "N-[2-(Diphenylphosphino)phenyl]benzamide". Acta Crystallographica Section E Structure Reports Online 63, nr 10 (15.09.2007): o4016. http://dx.doi.org/10.1107/s1600536807042092.

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41

Decken, Andreas, Johanna M. Blacquiere, Christopher M. Vogels i Stephen A. Westcott. "N-[(Benzylcarbamoyl)(phenyl)methyl]-N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]benzamide". Acta Crystallographica Section E Structure Reports Online 62, nr 6 (10.05.2006): o2207—o2208. http://dx.doi.org/10.1107/s1600536806016126.

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42

Kawski, Alfons, Barbara Bartoszewicz i Cerylia Strzalkowska. "Elektrische Dipolmomente von N-Phenyl-α-naphthylamin und N-Phenyl-β-naphthylamin im Anregungszustand". Zeitschrift für Chemie 12, nr 7 (1.09.2010): 275. http://dx.doi.org/10.1002/zfch.19720120719.

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43

Li, Xin-Gui, Mei-Rong Huang, Zhi-Liang Zhu, Yi Jin i Xue-Song Wang. "Structure and thermal degradation of poly(N-phenyl acrylamide) and poly(N-phenyl methacrylamide)". Journal of Applied Polymer Science 88, nr 4 (14.02.2003): 1065–71. http://dx.doi.org/10.1002/app.11824.

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44

Hoffmann, Siegfried, Nguyen Thi Hanh, Kerstin Mandl, Gerald Brezesinski i Eckhard Günther. "Vinamid-Mesogene - [4-n-Alkoxy-phenyl]-[β-(4-n-alkoxy-phenyl)amino-vinyl]-ketone". Zeitschrift für Chemie 26, nr 3 (31.08.2010): 103–4. http://dx.doi.org/10.1002/zfch.19860260312.

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45

Gataullin, Rail R., Ivan S. Afon'kin, Akhnaf A. Fatykhov, Leonid V. Spirikhin i Il'dus B. Abdrakhmanov. "ChemInform Abstract: Iodocyclization of N-(2-Nitrophenyl)- and N-Phenyl-N′-[2-(alk-1-enyl)phenyl]ethanimidamides." ChemInform 33, nr 11 (22.05.2010): no. http://dx.doi.org/10.1002/chin.200211037.

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46

Basenko, S. V., L. E. Zelenkov, M. G. Voronkov i A. I. Albanov. "Phenyl(trimethylsiloxy)fluorosiloxanes PhSi(OSiMe3) n F3−n". Russian Journal of General Chemistry 79, nr 6 (czerwiec 2009): 1083–85. http://dx.doi.org/10.1134/s1070363209060073.

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47

Pang, Tao, Yi-chong Sun i Jian-ming Zhang. "N-Phenyl-N-(3-phenylprop-2-ynyl)aniline". Acta Crystallographica Section E Structure Reports Online 65, nr 10 (26.09.2009): o2555. http://dx.doi.org/10.1107/s1600536809037866.

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48

Yusof, Mohd Sukeri Mohd, Nur Farhana Embong, Suhana Arshad i Ibrahim Abdul Razak. "N-(4-Chlorobutanoyl)-N′-[2-(trifluoromethyl)phenyl]thiourea". Acta Crystallographica Section E Structure Reports Online 68, nr 4 (10.03.2012): o1029. http://dx.doi.org/10.1107/s1600536812008859.

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In the title compound, C12H12ClF3N2OS, the dihedral angle between the benzene ring and the thiourea fragment is 69.41 (5)°. The thiourea N—H atoms adopt ananticonformation, such that one of them forms an intramolecular N—H...O hydrogen bond, generating anS(6) ring. In the crystal, both N—H groups form inversion dimers, oneviaa pair of N—H...S hydrogen bonds and oneviaa pair of N—H...O hydrogen bonds. These lead toR22(8) andR22(12) loops, respectively. Weak C—H...Cl, C—H...F, C—H...S and π–π [centroid–centroid separation = 3.7098 (6)Å and slippage = 1.853 Å] interactions also occur.
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49

Miyamoto, Hisakazu, Genta Yamauchi, Takuya Ueno i Hidehiro Uekusa. "Crystal structure of N-isopropyl-N-(phenyl)phenylglyoxylamide". Acta Crystallographica Section E Crystallographic Communications 74, nr 11 (12.10.2018): 1574–76. http://dx.doi.org/10.1107/s2056989018013762.

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The title compound [systematic name: 2-oxo-N,2-diphenyl-N-(propan-2-yl)acetamide], C17H17NO2, was synthesized and its photoreactive properties in the crystalline state were investigated. In the molecule, the carbonyl group attached to the phenyl ring adopts an s-trans configuration with respect to the isopropyl group. Moreover, the distance between the C atom of the carbonyl group and the N-bound C atom of the isopropyl group is 3.845 (2) Å, which is much longer than 3.2 Å, the threshold for photoreactions to take place in the molecule. As a result, the crystal did not photoreact upon UV light irradiation. In the crystal, the molecules are linked via weak intermolecular C—H...O hydrogen bonds, forming a layer structure parallel to the ab plane.
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Yuan, Chunlan. "N-(2,4-Dinitrophenyl)-N′-[nitro(phenyl)methylene]hydrazine". Acta Crystallographica Section E Structure Reports Online 64, nr 12 (8.11.2008): o2297. http://dx.doi.org/10.1107/s1600536808036179.

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