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Journal articles on the topic 'N-Salicylideneaniline'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Kim, Ji Ung, and Yeong Hae Kim. "Luminescence Intensity Change Using N-Carbamoylglycine, N-Salicylideneaniline and Metal ions." Journal of the Korean Chemical Society 46, no. 6 (2002): 502–8. http://dx.doi.org/10.5012/jkcs.2002.46.6.502.

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2

Goto, T., and Y. Tashiro. "Photochromism of N-salicylideneaniline single crystal." Journal of Luminescence 72-74 (June 1997): 921–22. http://dx.doi.org/10.1016/s0022-2313(96)00243-8.

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3

Silva, F. S., P. H. Suegama, W. P. Silva, et al. "Effect of Different Dopants in Films TEOS/MPTS Used to Protect the Carbon Steel." Materials Science Forum 805 (September 2014): 167–71. http://dx.doi.org/10.4028/www.scientific.net/msf.805.167.

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Schiff bases m-toluene N-Salicylideneaniline (m-TOL), (B) m-nitro-N- Salicylideneaniline (m-NTR) and (C) m-methoxy-N-salicylideneaniline (m-MTX) and cerium ions were studied added to 3.5 wt.% NaCl solution and added to the hybrid film based tetraethoxysilane (TEOS) e 3-methacryloxypropyltrimethoxysilane (MPTS). The polarization measurements showed lower current densities for the steel in NaCl with m-MTX, indicating that the m-MTX may be acting as an inhibitor. The hybrid films were doped with the m-MTX, Ce (III) or Ce (IV). Electrochemical measurements of open circuit potential (EOC), polariza

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4

Pathak, Suraj Kumar, Subrata Nath, Joydip De, Santanu Kumar Pal, and Ammathnadu S. Achalkumar. "The effect of regioisomerism on the mesomorphic and photophysical behavior of oxadiazole-based tris(N-salicylideneaniline)s: synthesis and characterization." New Journal of Chemistry 41, no. 18 (2017): 9908–17. http://dx.doi.org/10.1039/c7nj01766a.

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5

Pathak, Suraj Kumar, Subrata Nath, Joydip De, Santanu Kumar Pal, and Ammathnadu S. Achalkumar. "Contrasting effects of heterocycle substitution and branched tails in the arms of star-shaped molecules." New Journal of Chemistry 41, no. 11 (2017): 4680–88. http://dx.doi.org/10.1039/c7nj00911a.

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6

Sugiyama, Haruki, Kohei Johmoto, Akiko Sekine, and Hidehiro Uekusa. "Reversible on/off switching of photochromic properties in N-salicylideneaniline co-crystals by heating and humidification." CrystEngComm 21, no. 20 (2019): 3170–75. http://dx.doi.org/10.1039/c9ce00442d.

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7

Jagadesan, Pradeepkumar, Grace Eder, and Psaras L. McGrier. "The excited-state intramolecular proton transfer properties of three imine-linked two-dimensional porous organic polymers." Journal of Materials Chemistry C 5, no. 23 (2017): 5676–79. http://dx.doi.org/10.1039/c7tc00123a.

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8

Johmoto, Kohei, Takashi Ishida, Akiko Sekine, Hidehiro Uekusa, and Yuji Ohashi. "Relation between photochromic properties and molecular structures in salicylideneaniline crystals." Acta Crystallographica Section B Structural Science 68, no. 3 (2012): 297–304. http://dx.doi.org/10.1107/s0108768112010993.

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The crystal structures of the salicylideneaniline derivatives N-salicylidene-4-tert-butyl-aniline (1), N-3,5-di-tert-butyl-salicylidene-3-methoxyaniline (2), N-3,5-di-tert-butyl-salicylidene-3-bromoaniline (3), N-3,5-di-tert-butyl-salicylidene-3-chloroaniline (4), N-3,5-di-tert-butyl-salicylidene-4-bromoaniline (5), N-3,5-di-tert-butyl-salicylidene-aniline (6), N-3,5-di-tert-butyl-salicylidene-4-carboxyaniline (7) and N-salicylidene-2-chloroaniline (8) were analyzed by X-ray diffraction analysis at ambient temperature to investigate the relationship between their photochromic properties and mo

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9

Yin, Ming, Yuichiro Haramoto, and Masato Nanasawa. "Photochromism of 2-Chloro-N-salicylideneaniline in Amorphous Polymer Solids." Polymer Journal 27, no. 2 (1995): 136–40. http://dx.doi.org/10.1295/polymj.27.136.

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10

Li, Ziyong, Chan Zhang, Shuyuan Huang, Sisi Li, Jun Yin, and Sheng Hua Liu. "Synthesis and Properties of Photochromic Diarylethene Containing N-Salicylideneaniline Units." Molecular Crystals and Liquid Crystals 557, no. 1 (2012): 84–89. http://dx.doi.org/10.1080/15421406.2011.636230.

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11

Shen, M. Y., L. Z. Zhao, T. Goto, and A. Mordzinski. "Polarization dependence of photochromism in an N-salicylideneaniline single crystal." Journal of Chemical Physics 112, no. 5 (2000): 2490–97. http://dx.doi.org/10.1063/1.480815.

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12

Yelamaggad, Channabasaveshwar V., Ammathnadu S. Achalkumar, D. S. Shankar Rao, and S. Krishna Prasad. "Luminescent, Liquid Crystalline Tris(N-salicylideneaniline)s: Synthesis and Characterization." Journal of Organic Chemistry 74, no. 8 (2009): 3168–71. http://dx.doi.org/10.1021/jo9001933.

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13

Otsubo, Nobuto, Chie Okabe, Hirotoshi Mori, et al. "Excited-state intramolecular proton transfer in photochromic jet-cooled N-salicylideneaniline." Journal of Photochemistry and Photobiology A: Chemistry 154, no. 1 (2002): 33–39. http://dx.doi.org/10.1016/s1010-6030(02)00306-4.

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14

Fang, Wei-Hai, Xiao-Zeng You, and Zhen Yin. "Theoretical studies on the photochromic processes of 4-bromo-N-salicylideneaniline." Theoretica Chimica Acta 92, no. 5 (1995): 297–303. http://dx.doi.org/10.1007/bf01113869.

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15

Fan, Zhi-Qiang, Zhen-Hua Zhang, Xiao-Qing Deng, Gui-Ping Tang, and Ke-Qiu Chen. "Reversible switching in an N-salicylideneaniline molecular device induced by hydrogen transfer." Organic Electronics 13, no. 12 (2012): 2954–58. http://dx.doi.org/10.1016/j.orgel.2012.08.019.

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16

Yamina, Boukraa. "Extractive separation of Cu2+–Co2+ and Ni2+–Co2+ mixtures using N-salicylideneaniline." Russian Journal of Physical Chemistry A 90, no. 13 (2016): 2642–45. http://dx.doi.org/10.1134/s0036024416130033.

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17

Hiremath, Uma S. "Liquid crystalline bis(N-salicylideneaniline)s: synthesis and thermal behavior of constitutional isomers." Tetrahedron Letters 54, no. 26 (2013): 3419–23. http://dx.doi.org/10.1016/j.tetlet.2013.04.071.

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18

Moosavi-Tekyeh, Zainab, and Najmeh Dastani. "Intramolecular hydrogen bonding in N-salicylideneaniline: FT-IR spectrum and quantum chemical calculations." Journal of Molecular Structure 1102 (December 2015): 314–22. http://dx.doi.org/10.1016/j.molstruc.2015.09.001.

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19

Kawato, Toshio, Kiichi Amimoto, Hiroshi Maeda, Hiroyuki Koyama, and Hajime Kanatomi. "Photochromism of Guest N-Salicylideneaniline in the Rooms of Host Bile Acid Derivatives." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 345, no. 1 (2000): 57–62. http://dx.doi.org/10.1080/10587250008023895.

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20

Hetmańczyk, Łukasz, Eugene A. Goremychkin, Janusz Waliszewski, et al. "Spectroscopic Identification of Hydrogen Bond Vibrations and Quasi-Isostructural Polymorphism in N-Salicylideneaniline." Molecules 26, no. 16 (2021): 5043. http://dx.doi.org/10.3390/molecules26165043.

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The ortho-hydroxy aryl Schiff base 2-[(E)-(phenylimino)methyl]phenol and its deutero-derivative have been studied by the inelastic incoherent neutron scattering (IINS), infrared (IR) and Raman experimental methods, as well as by Density Functional Theory (DFT) and Density-Functional Perturbation Theory (DFPT) simulations. The assignments of vibrational modes within the 3500–50 cm−1 spectral region made it possible to state that the strong hydrogen bond in the studied compound can be classified as the so-called quasi-aromatic bond. The isotopic substitution supplemented by the results of DFT ca

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21

Blumenthal, T., M. Dosen, RG Gillis, and QN Porter. "Rearrangements in the Molecular Ions of Some ortho-Substituted Schiff Bases." Australian Journal of Chemistry 46, no. 6 (1993): 895. http://dx.doi.org/10.1071/ch9930895.

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Under electron ionization conditions, the ortho-substituted Schiff bases N-benzylidene-o-toluidine (1a), N-(o-methylbenzylidene)aniline (1b), N-salicylideneaniline (1c) and N-(o-methoxybenzylidene)aniline (1d) give fragment ions which have been shown by collision-activated mass-analysed ion kinetic energy spectra to have the structure of the protonated molecular ions of indole (2), benzofuran (3), and 1,2-benzisoxazole (4). The molecular ion of N-(o-methylbenzylidene)-o-toluidine (1f) gives as fragment ions not only the protonated molecular ion (2) of indole and the tropylium ion but also the

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22

ZHAO LI-ZHU, SHEN MENG-YAN, and T. GOTO. "GROWING N-SALICYLIDENEANILINE (SA) SINGLE CRYSTAL BY PHYSICAL VAPOUR DEPOSITATION AND ITS POLARIZATION PROPERTY." Acta Physica Sinica 50, no. 8 (2001): 1540. http://dx.doi.org/10.7498/aps.50.1540.

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23

Shahab, Siyamak, Liudmila Filippovich, M. Aharodnikova, et al. "Photochromic properties of the N-Salicylideneaniline in Polyvinyl Butyral matrix: Experimental and theoretical investigations." Journal of Molecular Structure 1134 (April 2017): 530–37. http://dx.doi.org/10.1016/j.molstruc.2016.12.038.

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24

Vieweger, Mario, Xuan Jiang, Young-Kwan Lim, Junyong Jo, Dongwhan Lee та Bogdan Dragnea. "Conformationally Dynamic π-Conjugation: Probing Structure–Property Relationships of Fluorescent Tris(N-salicylideneaniline)s". Journal of Physical Chemistry A 115, № 46 (2011): 13298–308. http://dx.doi.org/10.1021/jp2079583.

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25

Mercier, Gabriel M., Koen Robeyns, Nikolay Tumanov, Benoit Champagne, Johan Wouters, and Tom Leyssens. "New Insights into Photochromic Properties of N-Salicylideneaniline Derivatives Using a Cocrystal Engineering Approach." Crystal Growth & Design 19, no. 10 (2019): 5544–56. http://dx.doi.org/10.1021/acs.cgd.9b00363.

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26

Hiremath, Uma S. "Constitutional bis(N-salicylideneaniline)s as new class of mesogens: synthesis and thermal properties." Liquid Crystals 41, no. 1 (2013): 44–55. http://dx.doi.org/10.1080/02678292.2013.834080.

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27

Carletta, Andrea, Nikolay Tumanov, Tom Leyssens, Benoît Champagne, and Johan Wouters. "Altering the solid-state photochromic behaviour of N-salicylideneaniline molecular switches by co-crystallization." Acta Crystallographica Section A Foundations and Advances 74, a2 (2018): e356-e356. http://dx.doi.org/10.1107/s205327331808988x.

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28

Achalkumar, Ammathnadu S., Uma S. Hiremath, D. S. Shankar Rao, S. Krishna Prasad, and Channabasaveshwar V. Yelamaggad. "Self-Assembly of Hekates-Tris(N-salicylideneaniline)s into Columnar Structures: Synthesis and Characterization." Journal of Organic Chemistry 78, no. 2 (2012): 527–44. http://dx.doi.org/10.1021/jo302332u.

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29

Mittapalli, Sudhir, D. Sravanakumar Perumalla, and Ashwini Nangia. "Mechanochemical synthesis ofN-salicylideneaniline: thermosalient effect of polymorphic crystals." IUCrJ 4, no. 3 (2017): 243–50. http://dx.doi.org/10.1107/s2052252517004043.

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Polymorphs of the dichloro derivative ofN-salicylideneaniline exhibit mechanical responses such as jumping (Forms I and III) and exploding (Form II) in its three polymorphs. The molecules are connectedviathe amide N—H...O dimer synthon and C—Cl...O halogen bond in the three crystal structures. A fourth high-temperature Form IV was confirmed by variable-temperature single-crystal X-ray diffraction at 180°C. The behaviour of jumping exhibited by the polymorphic crystals of Forms I and III is due to the layered sheet morphology and the transmission of thermal stress in a single direction, compare

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30

Hoshino, Naomi, Hikari Murakami, Yoshio Matsunaga, Tamotsu Inabe, and Yusei Maruyama. "Liquid crystalline copper(II) complexes of N-salicylideneaniline derivatives. Mesomorphic properties and a crystal structure." Inorganic Chemistry 29, no. 6 (1990): 1177–81. http://dx.doi.org/10.1021/ic00331a014.

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31

Sugiyama, Haruki, Kohei Johmoto, Akiko Sekine, and Hidehiro Uekusa. "In-Situ Photochromism Switching with Crystal Jumping through the Deammoniation of N-Salicylideneaniline Ammonium Salt." Crystal Growth & Design 19, no. 8 (2019): 4324–31. http://dx.doi.org/10.1021/acs.cgd.9b00039.

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32

Quertinmont, Jean, Tom Leyssens, Johan Wouters, and Benoît Champagne. "Periodic DFT Study of the Effects of Co‐Crystallization on a N‐Salicylideneaniline Molecular Switch." ChemPhysChem 20, no. 19 (2019): 2434–42. http://dx.doi.org/10.1002/cphc.201900463.

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33

Quertinmont, Jean, Tom Leyssens, Johan Wouters, and Benoît Champagne. "Periodic DFT Study of the Effects of Co‐Crystallization on a N‐Salicylideneaniline Molecular Switch." ChemPhysChem 20, no. 19 (2019): 2402. http://dx.doi.org/10.1002/cphc.201900885.

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34

Okabe, Chie, Takakazu Nakabayashi, Yoshiya Inokuchi, Nobuyuki Nishi, and Hiroshi Sekiya. "Ultrafast excited-state dynamics in photochromic N-salicylideneaniline studied by femtosecond time-resolved REMPI spectroscopy." Journal of Chemical Physics 121, no. 19 (2004): 9436–42. http://dx.doi.org/10.1063/1.1801991.

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35

Achalkumar, Ammathnadu S., B. N. Veerabhadraswamy, Uma S. Hiremath, Doddamane S. Shankar Rao, Subbarao Krishna Prasad, and Channabasaveshwar V. Yelamaggad. "Photoluminescent discotic liquid crystals derived from tris( N -salicylideneaniline) and stilbene conjugates: Structure–property correlations." Dyes and Pigments 132 (September 2016): 291–305. http://dx.doi.org/10.1016/j.dyepig.2016.05.010.

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36

Sekine, Akiko, Yuta Yamazaki, Kohei Johmoto, and Hidehiro Uekusa. "Control of Photochromism in Crystalline-State in Dual Photoisomeric Complexes." Acta Crystallographica Section A Foundations and Advances 70, a1 (2014): C920. http://dx.doi.org/10.1107/s2053273314090792.

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Photochromic materials have attracted attention in recent years, however, in situ control of the photochromic reactivities still challenging. In order to realize dynamic control of photochromic property in crystal, we designed and created new dual photoisomeric type cobaloxime complexes, in which the reactivity of photochromic ligand changes by contact with surrounding photoreactive ligands. In this study, salicylideneaniline derivatives (SAP) are used as photochromic ligands, and the relationships between their photochromic reactivity and structural changes induced by crystalline-state photoi

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37

Yelamaggad, Channabasaveshwar V., Ammathnadu S. Achalkumar, D. S. Shankar Rao, and S. Krishna Prasad. "A New Class of Discotic Mesogens Derived from Tris(N-salicylideneaniline)s Existing inC3handCsKeto-Enamine Forms." Journal of Organic Chemistry 72, no. 22 (2007): 8308–18. http://dx.doi.org/10.1021/jo0712650.

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38

Jagadesan, Pradeepkumar, Tyler Whittemore, Toni Beirl, Claudia Turro, and Psaras L. McGrier. "Excited-State Intramolecular Proton-Transfer Properties of Three Tris(N-Salicylideneaniline)-Based Chromophores with Extended Conjugation." Chemistry - A European Journal 23, no. 4 (2016): 917–25. http://dx.doi.org/10.1002/chem.201604315.

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39

Mambourg, Kalina, Laurie Bodart, Nikolay Tumanov, Steve Lanners, and Johan Wouters. "Synthesis, crystal structure and conformational analysis of an unexpected [1,5]dithiocine product of aminopyridine and thiovanillin." Acta Crystallographica Section C Structural Chemistry 76, no. 3 (2020): 205–11. http://dx.doi.org/10.1107/s2053229620000996.

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The condensation reaction of 2-mercapto-3-methoxybenzaldehyde with 3-aminopyridine afforded an unexpected N-alkylated [1,5]dithiocine instead of the N-salicylideneaniline. The proposed mechanism for this condensation involves a strong intramolecular hydrogen bond between the thiol and the amine groups, leading to a second condensation. The corresponding product, i.e. 4,10-dimethoxy-13-(pyridin-3-yl)-6H,12H-6,12-epiminodibenzo[b,f][1,5]dithiocine methanol 0.463-solvate, C21H18N2O2S2·0.463CH3OH, was characterized by single-crystal X-ray diffraction analysis. The supramolecular structure shows π–

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40

Sugiyama, Haruki. "Photophysical property change of N-(5-bromo-salicylidene)-3-aminoethylpyridine monohydrated crystals via dehydration phase transition." Zeitschrift für Kristallographie - Crystalline Materials 236, no. 1-2 (2021): 43–50. http://dx.doi.org/10.1515/zkri-2020-0091.

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Abstract The crystals of N-salicylideneaniline (SA) and SA derivatives are classic functional materials that exhibit reversible colour changes (photochromism) and/or excited-state intramolecular proton transfer (ESIPT) fluorescence emission under ultraviolet (UV) light irradiation. In this study, a novel SA derivative was synthesised with an extended alkyl chain, N-(5-bromo-salicylidene)-3-aminoethylpyridine (5Br-SAEP). The photophysical properties of 5Br-SAEP were characterised in the crystalline state. The monohydrated crystal (1H) of 5Br-SAEP was dehydrated to form the anhydrous crystal (1A

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41

Valkonen, Arto, Erkki Kolehmainen, Aleksandra Grzegórska, Borys Ośmiałowski, Ryszard Gawinecki, and Kari Rissanen. "Two (E)-2-({[4-(dialkylamino)phenyl]imino}methyl)-4-nitrophenols." Acta Crystallographica Section C Crystal Structure Communications 68, no. 8 (2012): o279—o282. http://dx.doi.org/10.1107/s0108270112025589.

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The slow evaporation of analytical NMR samples resulted in the formation of crystals of (E)-2-({[4-(dimethylamino)phenyl]imino}methyl)-4-nitrophenol, C15H15N3O3, (I), and (E)-2-({[4-(diethylamino)phenyl]imino}methyl)-4-nitrophenol, C17H19N3O3, (II). Despite the small structural difference between these twoN-salicylideneaniline derivatives, they show different space groups and diverse molecular packing. The molecules of both compounds are close to being planar due to an intramolecular O—H...N hydrogen bond. The 4-alkylamino-substituted benzene ring is inclined at an angle of 13.44 (19)° in (I)

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42

Achalkumar, A. S., and C. V. Yelamaggad. "Light emitting, star-shaped tris(N-salicylideneaniline) discotic liquid crystals bearing trans-stilbene fluorophores: synthesis and characterization." Tetrahedron Letters 53, no. 52 (2012): 7108–12. http://dx.doi.org/10.1016/j.tetlet.2012.10.090.

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43

Liu, Hui-Yan, Hai-Ying Wang, Da-Qing Shi, and Jin-Lei Tian. "Synthesis and Crystal Structure of a Tetranuclear Cubane-like Nickel(II) Complex with 2-Hydroxymethyl-N-salicylideneaniline." Chinese Journal of Chemistry 24, no. 4 (2006): 518–20. http://dx.doi.org/10.1002/cjoc.200690099.

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44

SUGIYAMA, Haruki, and Hidehiro UEKUSA. "Crystal Structure and Chromic Properties of an Iron(II) Complex Salt of a N-Salicylideneaniline Derivative." X-ray Structure Analysis Online 36 (August 10, 2020): 31–32. http://dx.doi.org/10.2116/xraystruct.36.31.

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45

Amimoto, Kiichi, Hajime Kanatomi, Atsuyoshi Nagakari, Hisatane Fukuda, Hiroyuki Koyama, and Toshio Kawato. "Deuterium isotope effect on the solid-state thermal isomerization of photo-coloured cis-keto species of N-salicylideneaniline." Chemical Communications, no. 7 (March 5, 2003): 870–71. http://dx.doi.org/10.1039/b300830d.

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46

Yelamaggad, Channabasaveshwar V., Ammathnadu S. Achalkumar, Doddamane S. Shankar Rao, and Subbarao Krishna Prasad. "The first examples of optically active tris(N-salicylideneaniline)s: manifestation of chirality from molecules to fluid columnar phases." Journal of Materials Chemistry 17, no. 42 (2007): 4521. http://dx.doi.org/10.1039/b708432c.

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47

Garnovskii, D. A., A. Sousa, A. S. Antsyskkina, et al. "Electrosynthesis and studies of adducts of 2-amino-1-methylbenzimidazole with metal chelates based on 2-tosylamino-N-salicylideneaniline." Russian Chemical Bulletin 45, no. 8 (1996): 1988–92. http://dx.doi.org/10.1007/bf01457793.

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48

Zhang, Yong, and Zu-Hong Lu. "A multi-component molecular material design study on the correlation of electronic properties and proton transfer in N-salicylideneaniline derivatives." Materials Chemistry and Physics 63, no. 3 (2000): 188–95. http://dx.doi.org/10.1016/s0254-0584(99)00126-1.

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49

Quertinmont, Jean, Tom Leyssens, Johan Wouters, and Benoît Champagne. "Front Cover: Periodic DFT Study of the Effects of Co‐Crystallization on a N‐Salicylideneaniline Molecular Switch (ChemPhysChem 19/2019)." ChemPhysChem 20, no. 19 (2019): 2398. http://dx.doi.org/10.1002/cphc.201900886.

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50

Singh, D. P., A. K. Misra, A. S. Achalkumar, C. V. Yelamaggad, and M. Depriester. "Transmuting the blue fluorescence of hekates mesogens derived from tris(N-salicylideneaniline)s core via ZnS/ZnS:Mn2+ semiconductor quantum dots dispersion." Journal of Luminescence 210 (June 2019): 7–13. http://dx.doi.org/10.1016/j.jlumin.2019.02.009.

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