Статті в журналах з теми "Naphthalene Properties"
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El-Dossoki, Farid I. "Protonation and Solvation Thermodynamics of Some Naphthol Derivatives in KCl Aqueous Solution of Different Ionic Strengths." Journal of Chemistry 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/7234320.
Повний текст джерелаZhu, Jian Qing, Wei Wang, and Hui Ying Xu. "QSPR Models for the Physicochemical Properties of Polychlorinated Naphthalene Congeners." Advanced Materials Research 726-731 (August 2013): 440–43. http://dx.doi.org/10.4028/www.scientific.net/amr.726-731.440.
Повний текст джерелаBedi, Anjan, Linda J. W. Shimon, Benny Bogoslavsky, and Ori Gidron. "Easier to Twist than Bend: The Scope of the Bridge Formation Approach to Naphthalenophane Synthesis." Organic Materials 02, no. 04 (October 2020): 323–29. http://dx.doi.org/10.1055/s-0040-1721102.
Повний текст джерелаSrivastava, Umesh Chandra, and Shyamendra Pratap Singh. "Structural and Vibrational Properties of Solid Naphthalene (C10H8) by Use of VTBFS Model." Oriental Journal Of Chemistry 38, no. 3 (June 30, 2022): 762–65. http://dx.doi.org/10.13005/ojc/380329.
Повний текст джерелаChoi, Don-Soo, Mu-Young Kim, and Kyung-Woo Hyung. "Electrochemical and Spectrum Properties of 2,7-Naphthalene Ligand Compounds." Korean Journal of Materials Research 19, no. 9 (September 27, 2009): 510–15. http://dx.doi.org/10.3740/mrsk.2009.19.9.510.
Повний текст джерелаDos Santos, Andre, Marcos Dias, and David Antonelli. "Combustion Properties of Several Species of WoodCombustion Properties of Several Species of Wood." Chemistry & Chemical Technology 3, no. 3 (September 15, 2009): 177–82. http://dx.doi.org/10.23939/chcht03.03.177.
Повний текст джерелаBoinski, T., A. Cieszkowski, B. Rosa, B. Leśniewska, and A. Szumna. "Calixarenes with naphthalene units: calix[4]naphthalenes and hybrid[4]arenes." New Journal of Chemistry 40, no. 10 (2016): 8892–96. http://dx.doi.org/10.1039/c6nj01736c.
Повний текст джерелаWei, Sha Sha, Ren Jie Wang, and Gang Liu. "Synthesizes and Properties of a New Unsymmetrical Diarylethene with a Naphthalene Moiety." Advanced Materials Research 788 (September 2013): 219–22. http://dx.doi.org/10.4028/www.scientific.net/amr.788.219.
Повний текст джерелаMiroshnichenko, E. A., T. S. Kon’kova, Yu N. Matyushin, A. B. Vorob’ev, J. O. Inozemtsev, and A. V. Inozemtsev. "The Thermochemical Properties of Naphthalene Derivatives." Russian Journal of Physical Chemistry B 16, no. 2 (April 2022): 207–10. http://dx.doi.org/10.1134/s1990793122020191.
Повний текст джерелаVoloshchuk, Roman, Mariusz Tasior, Adina I. Ciuciu, Lucia Flamigni, and Daniel T. Gryko. "Corrole–imide dyads — Synthesis and optical properties." Journal of Porphyrins and Phthalocyanines 19, no. 01-03 (January 2015): 479–91. http://dx.doi.org/10.1142/s1088424615500339.
Повний текст джерелаKumar, Vipin B., Cassandra L. Fleming, Sai Shruthi Murali, Paul A. Hume, Nathaniel J. L. K. Davis, Tilo Söhnel, and Erin M. Leitao. "The photophysical properties of naphthalene bridged disilanes." RSC Advances 11, no. 35 (2021): 21343–50. http://dx.doi.org/10.1039/d1ra02961d.
Повний текст джерелаIchino, Rina, Atsuya Momotake, and Tatsuo Arai. "Photochemical properties of enediyne-cored dendrimers bearing naphthalenes at the periphery." Canadian Journal of Chemistry 97, no. 2 (February 2019): 112–19. http://dx.doi.org/10.1139/cjc-2018-0128.
Повний текст джерелаLasitha, P., and Edamana Prasad. "Orange red emitting naphthalene diimide derivative containing dendritic wedges: aggregation induced emission (AIE) and detection of picric acid (PA)." RSC Advances 5, no. 52 (2015): 41420–27. http://dx.doi.org/10.1039/c5ra04857e.
Повний текст джерелаLi, Jinjin, Zhi Zheng, Xiao Cui, Yunhu Liu, Ting Fan, Yueyue Liu, Dalei Chang, and Dezheng Yang. "Decomposition of Naphthalene by Dielectric Barrier Discharge in Conjunction with a Catalyst at Atmospheric Pressure." Catalysts 12, no. 7 (July 5, 2022): 740. http://dx.doi.org/10.3390/catal12070740.
Повний текст джерелаAl Kobaisi, Mohammad, Sidhanath V. Bhosale, Kay Latham, Aaron M. Raynor, and Sheshanath V. Bhosale. "Functional Naphthalene Diimides: Synthesis, Properties, and Applications." Chemical Reviews 116, no. 19 (August 26, 2016): 11685–796. http://dx.doi.org/10.1021/acs.chemrev.6b00160.
Повний текст джерелаZheng, Daoyuan, Mingxing Zhang, and Guangjiu Zhao. "The promotion effects of thionation and isomerization on charge carrier mobility in naphthalene diimide crystals." Phys. Chem. Chem. Phys. 19, no. 41 (2017): 28175–81. http://dx.doi.org/10.1039/c7cp03787b.
Повний текст джерелаNechaev, Lev V., Olga N. Tchaikovskaya, Elizaveta V. Maltseva, and Natalya V. Yudina. "Development of a New Technology of Environmental Purification from Naphthalene." Advanced Materials Research 1085 (February 2015): 154–60. http://dx.doi.org/10.4028/www.scientific.net/amr.1085.154.
Повний текст джерелаDu, Chuan Wei, and Guo Zhong Li. "Study on Effect and Action Mechanism of Different Superplasticizer on Properties of Titanium Gypsum." Applied Mechanics and Materials 468 (November 2013): 24–27. http://dx.doi.org/10.4028/www.scientific.net/amm.468.24.
Повний текст джерелаCimerman, Richard, Mária Cíbiková, Leonid Satrapinskyy, and Karol Hensel. "The Effect of Packing Material Properties on Tars Removal by Plasma Catalysis." Catalysts 10, no. 12 (December 17, 2020): 1476. http://dx.doi.org/10.3390/catal10121476.
Повний текст джерелаJia, Hongxing, Yuyue Gao, Qiang Huang, Shengsheng Cui, and Pingwu Du. "Facile three-step synthesis and photophysical properties of [8]-, [9]-, and [12]cyclo-1,4-naphthalene nanorings via platinum-mediated reductive elimination." Chemical Communications 54, no. 8 (2018): 988–91. http://dx.doi.org/10.1039/c7cc07370d.
Повний текст джерелаNencetti, Susanna, Lidia Ciccone, Armando Rossello, Elisa Nuti, Claudio Milanese, and Elisabetta Orlandini. "Synthesis and cycloxygenase inhibitory properties of new naphthalene-methylsulfonamido, naphthalene-methylsulfonyl and tetrahydronaphthalen-methylsulfonamido compounds." Journal of Enzyme Inhibition and Medicinal Chemistry 30, no. 3 (August 4, 2014): 406–12. http://dx.doi.org/10.3109/14756366.2014.940937.
Повний текст джерелаLiu, Jian-Jun, Teng Liu, Shu-Biao Xia, Chi-Xian He, Fei-Xiang Cheng, Mei-Jin Lin, and Chang-Cang Huang. "Cocrystals of naphthalene diimide with naphthalene derivatives: A facile approach to tune the luminescent properties." Dyes and Pigments 149 (February 2018): 59–64. http://dx.doi.org/10.1016/j.dyepig.2017.09.058.
Повний текст джерелаMurakami, Mutsuaki, Susumu Yoshimura, and Sumio Iijima. "Structural properties of graphitized poly‐peri‐naphthalene whiskers." Applied Physics Letters 48, no. 6 (February 10, 1986): 390–92. http://dx.doi.org/10.1063/1.96561.
Повний текст джерелаKokan, Zoran, Berislav Perić, Janja Makarević, Goran Štefanić, Leo Frkanec, and Srećko I. Kirin. "Crystal structure and gelation properties of naphthalene bioconjugates." Acta Crystallographica Section A Foundations and Advances 71, a1 (August 23, 2015): s450—s451. http://dx.doi.org/10.1107/s2053273315093389.
Повний текст джерелаLeu, Tsu-Shang, and Chun-Shan Wang. "Synthesis and properties of copolyimides containing naphthalene group." Polymer 43, no. 25 (January 2002): 7069–74. http://dx.doi.org/10.1016/s0032-3861(02)00530-x.
Повний текст джерелаFeng, Jinwu, Xiaopeng Chen, Qingchuan Han, Hongbo Wang, Ping Lu, and Yanguang Wang. "Naphthalene-based fluorophores: Synthesis characterization, and photophysical properties." Journal of Luminescence 131, no. 12 (December 2011): 2775–83. http://dx.doi.org/10.1016/j.jlumin.2011.06.027.
Повний текст джерелаCheon, Jong-Woo, Chil-Won Lee, Myoung-Seon Gong, and Neri Geum. "Chemiluminescent properties of blue fluorophores containing naphthalene unit." Dyes and Pigments 61, no. 1 (April 2004): 23–30. http://dx.doi.org/10.1016/j.dyepig.2003.08.008.
Повний текст джерелаKim, Yeong-Eun, and Jong-Wook Park. "Luminescent Properties of Pentacene Derivatives with Naphthalene Moiety." Molecular Crystals and Liquid Crystals 444, no. 1 (February 1, 2006): 137–43. http://dx.doi.org/10.1080/15421400500365318.
Повний текст джерелаWang, Chun-Shan, and Hann-Jang Hwang. "Synthesis and properties of novel naphthalene-containing bismaleimides." Journal of Applied Polymer Science 60, no. 6 (May 9, 1996): 857–63. http://dx.doi.org/10.1002/(sici)1097-4628(19960509)60:6<857::aid-app8>3.0.co;2-i.
Повний текст джерелаRabanzo-Castillo, Kristel M., Muhammad Hanif, Tilo Söhnel, and Erin M. Leitao. "Synthesis, characterisation and electronic properties of naphthalene bridged disilanes." Dalton Transactions 48, no. 37 (2019): 13971–80. http://dx.doi.org/10.1039/c9dt03058a.
Повний текст джерелаGutiérrez, Mario, Félix Sánchez, and Abderrazzak Douhal. "Spectral and dynamical properties of a Zr-based MOF." Physical Chemistry Chemical Physics 18, no. 7 (2016): 5112–20. http://dx.doi.org/10.1039/c5cp04436g.
Повний текст джерелаParales, Rebecca E., Juanito V. Parales, and David T. Gibson. "Aspartate 205 in the Catalytic Domain of Naphthalene Dioxygenase Is Essential for Activity." Journal of Bacteriology 181, no. 6 (March 15, 1999): 1831–37. http://dx.doi.org/10.1128/jb.181.6.1831-1837.1999.
Повний текст джерелаGündüz qızı Əmirova, Günel. "Naftalan healing oil." NATURE AND SCIENCE 13, no. 08 (October 23, 2021): 36–39. http://dx.doi.org/10.36719/2707-1146/13/36-39.
Повний текст джерелаSong, Jin Mei, Yu Xiu Zhang, and Shu Quan Zhu. "Preparation and Properties of Modified Lignin Used as Additive of Brown Coal CWS." Advanced Materials Research 690-693 (May 2013): 1479–82. http://dx.doi.org/10.4028/www.scientific.net/amr.690-693.1479.
Повний текст джерелаWelsh, Thomas A., Olga Matsarskaia, Ralf Schweins, and Emily R. Draper. "Electronic and assembly properties of a water-soluble blue naphthalene diimide." New Journal of Chemistry 45, no. 31 (2021): 14005–13. http://dx.doi.org/10.1039/d1nj02557k.
Повний текст джерелаMarzuki, I., K. Nisaa, R. Asaf, R. Armus, M. Kamaruddin, A. Sapar, and A. Emelda. "Biodegradation mechanism of naphthalene using marine sponge symbiotic bacteria." IOP Conference Series: Earth and Environmental Science 890, no. 1 (October 1, 2021): 012020. http://dx.doi.org/10.1088/1755-1315/890/1/012020.
Повний текст джерелаBush, Benjamin F., та J. J. Lagowski. "The electrochemical properties of the (μ-η6,η6-naphthalene)dichromium compounds and bis(η6-naphthalene)chromium". Journal of Organometallic Chemistry 386, № 1 (квітень 1990): 37–50. http://dx.doi.org/10.1016/0022-328x(90)80255-x.
Повний текст джерелаAbu El-Rub, Ziad, Eddy Bramer, Samer Al-Gharabli, and Gerrit Brem. "Impact of Char Properties and Reaction Parameters on Naphthalene Conversion in a Macro-TGA Fixed Char Bed Reactor." Catalysts 9, no. 4 (March 28, 2019): 307. http://dx.doi.org/10.3390/catal9040307.
Повний текст джерелаRybakiewicz, Renata, Izabela Tszydel, Joanna Zapala, Lukasz Skorka, Damian Wamil, David Djurado, Jacques Pécaut, Jacek Ulanski, Malgorzata Zagorska, and Adam Pron. "New semiconducting naphthalene bisimides N-substituted with alkoxyphenyl groups: spectroscopic, electrochemical, structural and electrical properties." RSC Adv. 4, no. 27 (2014): 14089–100. http://dx.doi.org/10.1039/c4ra00052h.
Повний текст джерелаWu, Bin, Wen Hong Tao, Xing Hua Fu, and Fu Xing Wang. "Study on the Performance on Some Admixture of Sulphoaluminate Cement Waterproof Mortar." Applied Mechanics and Materials 740 (March 2015): 47–50. http://dx.doi.org/10.4028/www.scientific.net/amm.740.47.
Повний текст джерелаSilva, Wilson Ricardo Leal, Luiz Roberto Prudêncio, Alexandre Lima Oliveira, Gabriela Damo, and Eduardo Tochetto. "Influence of Air Temperature on the Performance of Different Water-Reducing Admixtures with Respect to the Properties of Fresh and Hardened Mortar." Advances in Civil Engineering 2010 (2010): 1–10. http://dx.doi.org/10.1155/2010/136768.
Повний текст джерелаTang, Xianxian, Taoxiang Liu, Han Li, Dongwang Yang, Liangjun Chen та Xinfeng Tang. "Notably enhanced thermoelectric properties of lamellar polypyrrole by doping with β-naphthalene sulfonic acid". RSC Advances 7, № 33 (2017): 20192–200. http://dx.doi.org/10.1039/c7ra02302b.
Повний текст джерелаNarayan, B., K. Nagura, T. Takaya, K. Iwata, A. Shinohara, H. Shinmori, H. Wang, et al. "The effect of regioisomerism on the photophysical properties of alkylated-naphthalene liquids." Physical Chemistry Chemical Physics 20, no. 5 (2018): 2970–75. http://dx.doi.org/10.1039/c7cp05584f.
Повний текст джерелаJeong, Jaemin, Fiaz Hussain, Sangwon Park, Soo-Jung Kang, and Jinhwan Kim. "High Thermal Stability, High Tensile Strength, and Good Water Barrier Property of Terpolyester Containing Biobased Monomer for Next-Generation Smart Film Application: Synthesis and Characterization." Polymers 12, no. 11 (October 23, 2020): 2458. http://dx.doi.org/10.3390/polym12112458.
Повний текст джерелаPandeeswar, M., Harshavardhan Khare, Suryanarayanarao Ramakumar, and T. Govindaraju. "Biomimetic molecular organization of naphthalene diimide in the solid state: tunable (chiro-) optical, viscoelastic and nanoscale properties." RSC Adv. 4, no. 39 (2014): 20154–63. http://dx.doi.org/10.1039/c3ra47257d.
Повний текст джерелаDikusar, E. I., L. I. Filippovich, S. N. Shahab, S. K. Petkevich, and S. G. Stepin. "(E,E)-diazomethines based on naphthalene-1,5-diamine and the study of their polarizrization properties." Proceedings of the National Academy of Sciences of Belarus, Chemical Series 56, no. 1 (March 19, 2020): 67–74. http://dx.doi.org/10.29235/1561-8331-2020-56-1-67-74.
Повний текст джерелаWeißenstein, Annike, Vincenzo Grande, Chantu R. Saha-Möller, and Frank Würthner. "Water-soluble naphthalene diimides: synthesis, optical properties, and colorimetric detection of biogenic amines." Organic Chemistry Frontiers 5, no. 18 (2018): 2641–51. http://dx.doi.org/10.1039/c8qo00611c.
Повний текст джерелаTaima, Masahiro, Yuka Ishida, and Tatsuo Arai. "Intramolecular energy transfer and photoisomerization in stilbene dendrimers." Canadian Journal of Chemistry 95, no. 9 (September 2017): 1013–23. http://dx.doi.org/10.1139/cjc-2017-0137.
Повний текст джерелаKalita, Kalyan Jyoti, Indrajit Giri, and Ratheesh K. Vijayaraghavan. "Influence of non-covalent interactions in dictating the polarity and mobility of charge carriers in a series of crystalline NDIs: a computational case study." RSC Advances 11, no. 53 (2021): 33703–13. http://dx.doi.org/10.1039/d1ra05274h.
Повний текст джерелаLing, Qing-Hui, Jun-Long Zhu, Yi Qin, and Lin Xu. "Naphthalene diimide- and perylene diimide-based supramolecular cages." Materials Chemistry Frontiers 4, no. 11 (2020): 3176–89. http://dx.doi.org/10.1039/d0qm00540a.
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