Статті в журналах з теми "Chiral Spacer"
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Guan, Weiming, Bao Li, and Lixin Wu. "Chiral hexamers of organically modified polyoxometalates via ionic complexation." Dalton Transactions 51, no. 11 (2022): 4541–48. http://dx.doi.org/10.1039/d2dt00093h.
Повний текст джерелаLi, L. S., and S. I. Stupp. "The chiral smectic H liquid crystalline structure of a comb-shaped side-chain polymer." Proceedings, annual meeting, Electron Microscopy Society of America 50, no. 1 (August 1992): 272–73. http://dx.doi.org/10.1017/s0424820100121764.
Повний текст джерелаRajakumar, Perumal, Beeran Senthilkumar, and Kannupal Srinivasan. "Synthesis of Azobenzenophanes with a Large Molecular Cavity." Australian Journal of Chemistry 59, no. 1 (2006): 75. http://dx.doi.org/10.1071/ch05254.
Повний текст джерелаYin, Lu, Yin Zhao, Meng Liu, Nianchen Zhou, Wei Zhang, and Xiulin Zhu. "Induction of supramolecular chirality by chiral solvation in achiral Azo polymers with different spacer lengths and push–pull electronic substituents: where will chiral induction appear?" Polymer Chemistry 8, no. 12 (2017): 1906–13. http://dx.doi.org/10.1039/c7py00130d.
Повний текст джерелаZhang, Yi Jun, Cai Xia Dong, Jun Chen, and Run Qiang Liu. "Cellulose Tris(3,5-Dimethylphenylcarbamate) Regioselectively Bonded to Small Pore Silica Gel as Chiral Stationary Phase for HPLC." Applied Mechanics and Materials 117-119 (October 2011): 1361–64. http://dx.doi.org/10.4028/www.scientific.net/amm.117-119.1361.
Повний текст джерелаZhao, Xuan-Hui, Xiaozong Hu, Meng-En Sun, Xi-Ming Luo, Chong Zhang, Gao-Song Chen, Xi-Yan Dong, and Shuang-Quan Zang. "An enantiomeric pair of 2D organic–inorganic hybrid perovskites with circularly polarized luminescence and photoelectric effects." Journal of Materials Chemistry C 10, no. 9 (2022): 3440–46. http://dx.doi.org/10.1039/d1tc05836c.
Повний текст джерелаGoh, Yit-Peng, Wan-Sinn Yam, Foo-Win Yip, and Gurumurthy Hegde. "Chiral Polymorphic Hydrazine-based Asymmetric Liquid Crystal Trimers with Resorcinol as Linking Group." Current Organic Synthesis 18, no. 4 (June 7, 2021): 352–65. http://dx.doi.org/10.2174/1570179418666210202123935.
Повний текст джерелаMarcos, Mercedes, Ana Omenat, Jose Luis Serrano, and Teresa Sierra. "Ferroelectric dimeric liquid crystals with a chiral flexible spacer." Chemistry of Materials 4, no. 2 (March 1992): 331–38. http://dx.doi.org/10.1021/cm00020a020.
Повний текст джерелаScherowsky, G., U. Müller, J. Springer, W. Trapp, A. M. Levelut, and P. Davidson. "Liquid-crystalline side chain polymers containing a chiral spacer unit exhibiting chiral smectic phases." Liquid Crystals 5, no. 4 (January 1989): 1297–306. http://dx.doi.org/10.1080/02678298908026435.
Повний текст джерелаChiellini, E., R. Po, S. Carrozzino, G. Galli, and B. Gallot. "Chiral Liquid-Crystalline Polymers. IX. The Effect of Chiral Spacer Structure in Thermotropic Polyesters." Molecular Crystals and Liquid Crystals Incorporating Nonlinear Optics 179, no. 1 (February 1990): 405–18. http://dx.doi.org/10.1080/00268949008055384.
Повний текст джерелаGhanem, Ashraf. "Enantioselective Gas Chromatographic Separation of Racemic N-alkylated Barbiturates: Application of C11-Chirasil-Dex as Chiral Stationary Phase in GC." Analytical Chemistry Insights 2 (January 2007): 117739010700200. http://dx.doi.org/10.4137/117739010700200003.
Повний текст джерелаSingh, Nirmal, and Lalit Sharma. "Synthesis of Carbohydrate Derived Non-ionic Gemini Surfactants and Study of Their Micellar and Reverse Micellar Behavior - A Review." Letters in Organic Chemistry 16, no. 8 (June 18, 2019): 607–14. http://dx.doi.org/10.2174/1570178616666190123124727.
Повний текст джерелаCsuk, René, and Anja Kern. "Synthesis of Rigid Cyclopropanoid Nucleoside Analogues." Zeitschrift für Naturforschung B 57, no. 10 (October 1, 2002): 1169–73. http://dx.doi.org/10.1515/znb-2002-1015.
Повний текст джерелаCsuk, René, and Gisela Thiede. "Synthesis of Spacered Nucleoside Analogues Comprising a Difluorocyclopropane Moiety." Zeitschrift für Naturforschung B 58, no. 9 (September 1, 2003): 853–60. http://dx.doi.org/10.1515/znb-2003-0907.
Повний текст джерелаBerthod, Alain, Chau-Dung Chang та Daniel W. Armstrong. "β-Cyclodextrin chiral stationary phases for liquid chromatography. Effect of the spacer arm on chiral recognition". Talanta 40, № 9 (вересень 1993): 1367–73. http://dx.doi.org/10.1016/0039-9140(93)80212-a.
Повний текст джерелаThirunarayanan, Ayyavu, and Perumal Rajakumar. "Synthesis, photophysical and electrochemical properties of chiral and achiral thiadiazolophanes." RSC Adv. 4, no. 45 (2014): 23433–39. http://dx.doi.org/10.1039/c4ra02672a.
Повний текст джерелаLiu, Gang, Yukie Saito, Daisuke Nishio-Hamane, Ajoy K. Bauri, Emmanuel Flahaut, Takahide Kimura, and Naoki Komatsu. "Structural discrimination of double-walled carbon nanotubes by chiral diporphyrin nanocalipers." J. Mater. Chem. A 2, no. 44 (2014): 19067–74. http://dx.doi.org/10.1039/c4ta04407j.
Повний текст джерелаEma, Tadashi, Shigeharu Misawa, Shuichi Nemugaki, Takashi Sakai, and Masanori Utaka. "New Optically Active Diporphyrin Having a Chiral Cyclophane as a Spacer." Chemistry Letters 26, no. 6 (June 1997): 487–88. http://dx.doi.org/10.1246/cl.1997.487.
Повний текст джерелаEma, T., S. Misawa, S. Nemugaki, T. Sakai, and M. Utaka. "New optically active diporphyrin having a chiral cyclophane as a spacer." Journal of Inorganic Biochemistry 67, no. 1-4 (July 1997): 416. http://dx.doi.org/10.1016/s0162-0134(97)80279-6.
Повний текст джерелаPoryvai, Anna, Alexej Bubnov, and Michal Kohout. "Chiral Photoresponsive Liquid Crystalline Materials Derived from Cyanoazobenzene Central Core: Effect of UV Light Illumination on Mesomorphic Behavior." Crystals 10, no. 12 (December 21, 2020): 1161. http://dx.doi.org/10.3390/cryst10121161.
Повний текст джерелаFaye, Valerie, Huu Tinh Nguyen, Valere Law, and Noel Isaert. "Influence of the Spacer in a Series of Chiral Non-Symmetric Dimesogens." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 301, no. 1 (August 1997): 183–88. http://dx.doi.org/10.1080/10587259708041765.
Повний текст джерелаMizuta, Kenichi, Makoto Katashima, Tomokazu Koga, Kazuhiro Yamabuki, Kenjiro Onimura, and Tsutomu Oishi. "Synthesis of chiral side-chain liquid crystalline polyacetylenes bearing succinic acid spacer." Polymer Bulletin 68, no. 3 (June 24, 2011): 623–34. http://dx.doi.org/10.1007/s00289-011-0558-0.
Повний текст джерелаWang, Dong, Tian Jun Liu, Chao Jun Li, and William T. Slaven. "A chiral conjugated oligomer based on 1,1′-binaphthol with 3,3′-acetylene spacer." Polymer Bulletin 39, no. 3 (September 1997): 265–70. http://dx.doi.org/10.1007/s002890050147.
Повний текст джерелаStarodubtsev, Evgenii. "Reflection and transmission of nanoresonators including bi-isotropic and metamaterial layers: opportunities to control and amplify chiral and nonreciprocal effects for nanophotonics applications." EPJ Applied Metamaterials 10 (2023): 5. http://dx.doi.org/10.1051/epjam/2023002.
Повний текст джерелаZhu, Zhao-Xia, Cong-Cong Luo, Ji-Wei Wang, Jian-She Hu, and Ying-Gang Jia. "Synthesis and properties of (−)-menthol-derived chiral liquid crystals by introducing adipoyloxy spacer between mesogenic core and chiral menthyl." Liquid Crystals 45, no. 10 (March 21, 2018): 1525–34. http://dx.doi.org/10.1080/02678292.2018.1453557.
Повний текст джерелаWang, Xiaobo, Haohua Li, and Ji Zhou. "Asymmetric Transmission in a Mie-Based Dielectric Metamaterial with Fano Resonance." Materials 12, no. 7 (March 27, 2019): 1003. http://dx.doi.org/10.3390/ma12071003.
Повний текст джерелаZhang, Guowen, Man Chao, Shuting Wang, Mengxia Zhu, Dou Wang, Guangsheng Pang, and Yanhui Shi. "Synthesis and Catalytic Activity of Chiral Dicarbene Dipalladium Complexes Incorporating the S-binaphthol Unit." Journal of Chemical Research 42, no. 1 (January 2018): 54–56. http://dx.doi.org/10.3184/174751918x15168768395864.
Повний текст джерелаJiao, Ti Feng, and Jing Xin Zhou. "Chiral Interfacial Assembly of a Trigonal Schiff Base Compound with TPPS in Organized Molecular Films." Applied Mechanics and Materials 236-237 (November 2012): 810–14. http://dx.doi.org/10.4028/www.scientific.net/amm.236-237.810.
Повний текст джерелаHeilmayer, Werner, Bianca Wallfisch, C. Oliver kappe, Curt Wentrup, Karsten Gloe, and Gert Kollenz. "Synthesis and Host-abilities of some New Corands Bearing Uncommon Chiral Spacer Units." Supramolecular Chemistry 15, no. 5 (July 1, 2003): 375–83. http://dx.doi.org/10.1080/1061027031000108848.
Повний текст джерелаEMA, T., S. MISAWA, S. NEMUGAKI, T. SAKAI, and M. UTAKA. "ChemInform Abstract: New Optically Active Diporphyrin Having a Chiral Cyclophane as a Spacer." ChemInform 28, no. 45 (August 3, 2010): no. http://dx.doi.org/10.1002/chin.199745124.
Повний текст джерелаRatih, Ratih, Hermann Wätzig, Azminah Azminah, Mufarreh Asmari, Benjamin Peters, and Sami El Deeb. "Immobilization of Chondroitin Sulfate A onto Monolithic Epoxy Silica Column as a New Chiral Stationary Phase for High-Performance Liquid Chromatographic Enantioseparation." Pharmaceuticals 14, no. 2 (January 27, 2021): 98. http://dx.doi.org/10.3390/ph14020098.
Повний текст джерелаLi, L. S., and S. I. Stupp. "A new type of liquid crystalline structure- The chiral smectic E phase of a comb-shaped polymer." Proceedings, annual meeting, Electron Microscopy Society of America 48, no. 4 (August 1990): 1100–1101. http://dx.doi.org/10.1017/s042482010017863x.
Повний текст джерелаWatanabe, Masami, and Kenso Soai. "Enantioselective addition of diethylzinc to aldehydes using chiral polymer catalysts possessing a methylene spacer." Journal of the Chemical Society, Perkin Transactions 1, no. 7 (1994): 837. http://dx.doi.org/10.1039/p19940000837.
Повний текст джерелаLuo, Cong-Cong, Qing-Lin Meng, Ji-Wei Wang, Gui-Yang Yan, and Ying-Gang Jia. "Effect of spacer length on mesomorphic behaviours of chiral liquid crystal compounds containing (-)-menthyl." Liquid Crystals 45, no. 12 (June 20, 2018): 1760–70. http://dx.doi.org/10.1080/02678292.2018.1485978.
Повний текст джерелаHernández, JoséV, Marta Almaraz, Cesar Raposo, Mercedes Martín, Anna Lithgow, Mercedes Crego, Cruz Caballero, and Joaquín R. Morán. "Chiral recognition of tartaric acid derivatives with chromenone-benzoxazole receptors and a spirobifluorene spacer." Tetrahedron Letters 39, no. 40 (October 1998): 7401–4. http://dx.doi.org/10.1016/s0040-4039(98)01606-2.
Повний текст джерелаHirst, Andrew R., David K. Smith, Martin C. Feiters, and Huub P. M. Geurts. "Two-Component Dendritic Gel: Effect of Spacer Chain Length on the Supramolecular Chiral Assembly." Langmuir 20, no. 17 (August 2004): 7070–77. http://dx.doi.org/10.1021/la048751s.
Повний текст джерелаYoshizawa, Atsushi, Yukie Soeda, and Isa Nishiyama. "Liquid-crystalline properties of a chiral twin material possessing a remarkably flexible central spacer." Journal of Materials Chemistry 5, no. 4 (1995): 675. http://dx.doi.org/10.1039/jm9950500675.
Повний текст джерелаMarcelis, Antonius T. M., Arie Koudijs, and Ernst J. R. Sudhölter. "Influence of spacer lengths on the properties of chiral triplet liquid crystals based on estradiol." Liquid Crystals 21, no. 1 (July 1996): 87–93. http://dx.doi.org/10.1080/02678299608033798.
Повний текст джерелаShankar, B. Vijai, and Archita Patnaik. "Chiral Discrimination of a Gemini-Type Surfactant with Rigid Spacer at the Air−Water Interface." Journal of Physical Chemistry B 111, no. 39 (October 2007): 11419–27. http://dx.doi.org/10.1021/jp074279i.
Повний текст джерелаMiao, Wangen, Dong Yang, and Minghua Liu. "Multiple-Stimulus-Responsive Supramolecular Gels and Regulation of Chiral Twists: The Effect of Spacer Length." Chemistry - A European Journal 21, no. 20 (April 1, 2015): 7562–70. http://dx.doi.org/10.1002/chem.201500097.
Повний текст джерелаGuldi, Dirk M., Francesco Giacalone, Gema de la Torre, José L. Segura, and Nazario Martín. "Topological Effects of a Rigid Chiral Spacer on the Electronic Interactions in Donor–Acceptor Ensembles." Chemistry - A European Journal 11, no. 24 (December 9, 2005): 7199–210. http://dx.doi.org/10.1002/chem.200500209.
Повний текст джерелаJia, Ying-Gang, Jian-She Hu, Dan Li, Qing-Bao Meng, and Xia Zhang. "Synthesis and phase behavior of chiral liquid crystalline polymeric networks derived from menthol." High Performance Polymers 24, no. 8 (June 28, 2012): 673–82. http://dx.doi.org/10.1177/0954008312449843.
Повний текст джерелаSeidel, Rüdiger W., та Iris M. Oppel. "Crystal structure of catena-poly[[diiodidomercury(II)]-μ-2,2′-dithiobis(pyridine N-oxide)-κ2 O:O′]". Acta Crystallographica Section E Crystallographic Communications 74, № 4 (2 березня 2018): 433–35. http://dx.doi.org/10.1107/s2056989018003055.
Повний текст джерелаItoh, Manabu, Masatoshi Tokita, Hiromitsu Hegi, Teruaki Hayakawa, Sungmin Kang, and Junji Watanabe. "Enhancement of the cholesteric induction power by macrocyclization in liquid crystal dimers with a chiral spacer." J. Mater. Chem. 21, no. 6 (2011): 1697–99. http://dx.doi.org/10.1039/c0jm03161e.
Повний текст джерелаInaki, Yoshiaki, Shigeki Kamo, and Mikiji Miyata. "Base-specific interaction of polymers containing adenine: effect of chiral spacer on the interaction with polynucleotide." Reactive and Functional Polymers 37, no. 1-3 (June 1998): 189–98. http://dx.doi.org/10.1016/s1381-5148(97)00118-1.
Повний текст джерелаSoai, Kenso, and Masami Watanabe. "New polymer bound chiral catalyst with methylene spacer for the enantioselective addition of diethylzinc to aldehydes." Tetrahedron: Asymmetry 2, no. 2 (January 1991): 97–100. http://dx.doi.org/10.1016/s0957-4166(00)80526-1.
Повний текст джерелаWallfisch, Bianca C., Tamara Egger, Werner Heilmayer, C. Oliver Kappe, Curt Wentrup, Karsten Gloe, Ferdinand Belaj, Gerd Klintschar, and Gert Kollenz. "2,6,9-Trioxabicyclo[3.3.1]nona-3,7-dienes and 2,4,6,8-Tetraoxaadamantanes: Novel Chiral Spacer Units in Macrocyclic Polyethers." Supramolecular Chemistry 14, no. 5 (July 1, 2002): 383–97. http://dx.doi.org/10.1080/1061027021000003430.
Повний текст джерелаHo Hyun, Myung, and Do Hun Kim. "Spacer length effect of a chiral stationary phase based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid." Chirality 16, no. 5 (2004): 294–301. http://dx.doi.org/10.1002/chir.20038.
Повний текст джерелаWATANABE, M., and K. SOAI. "ChemInform Abstract: Enantioselective Addition of Diethylzinc to Aldehydes Using Chiral Polymer Catalysts Possessing a Methylene Spacer." ChemInform 25, no. 32 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199432029.
Повний текст джерелаAbe, Yunosuke, Toshiki Aoki, Hongge Jia, Shingo Hadano, Takeshi Namikoshi, Yuriko Kakihana, Lijia Liu, Yu Zang, Masahiro Teraguchi, and Takashi Kaneko. "Chiral Teleinduction in Asymmetric Polymerization of 3,5-Bis(hydroxymethyl)phenylacetylene Having a Chiral Group via a Very Long and Rigid Spacer at 4-Position." Chemistry Letters 41, no. 3 (March 5, 2012): 244–46. http://dx.doi.org/10.1246/cl.2012.244.
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