Artículos de revistas sobre el tema "Chiral Spacer"
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Guan, Weiming, Bao Li y Lixin Wu. "Chiral hexamers of organically modified polyoxometalates via ionic complexation". Dalton Transactions 51, n.º 11 (2022): 4541–48. http://dx.doi.org/10.1039/d2dt00093h.
Texto completoLi, L. S. y 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, n.º 1 (agosto de 1992): 272–73. http://dx.doi.org/10.1017/s0424820100121764.
Texto completoRajakumar, Perumal, Beeran Senthilkumar y Kannupal Srinivasan. "Synthesis of Azobenzenophanes with a Large Molecular Cavity". Australian Journal of Chemistry 59, n.º 1 (2006): 75. http://dx.doi.org/10.1071/ch05254.
Texto completoYin, Lu, Yin Zhao, Meng Liu, Nianchen Zhou, Wei Zhang y 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, n.º 12 (2017): 1906–13. http://dx.doi.org/10.1039/c7py00130d.
Texto completoZhang, Yi Jun, Cai Xia Dong, Jun Chen y 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 (octubre de 2011): 1361–64. http://dx.doi.org/10.4028/www.scientific.net/amm.117-119.1361.
Texto completoZhao, Xuan-Hui, Xiaozong Hu, Meng-En Sun, Xi-Ming Luo, Chong Zhang, Gao-Song Chen, Xi-Yan Dong y 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, n.º 9 (2022): 3440–46. http://dx.doi.org/10.1039/d1tc05836c.
Texto completoGoh, Yit-Peng, Wan-Sinn Yam, Foo-Win Yip y Gurumurthy Hegde. "Chiral Polymorphic Hydrazine-based Asymmetric Liquid Crystal Trimers with Resorcinol as Linking Group". Current Organic Synthesis 18, n.º 4 (7 de junio de 2021): 352–65. http://dx.doi.org/10.2174/1570179418666210202123935.
Texto completoMarcos, Mercedes, Ana Omenat, Jose Luis Serrano y Teresa Sierra. "Ferroelectric dimeric liquid crystals with a chiral flexible spacer". Chemistry of Materials 4, n.º 2 (marzo de 1992): 331–38. http://dx.doi.org/10.1021/cm00020a020.
Texto completoScherowsky, G., U. Müller, J. Springer, W. Trapp, A. M. Levelut y P. Davidson. "Liquid-crystalline side chain polymers containing a chiral spacer unit exhibiting chiral smectic phases". Liquid Crystals 5, n.º 4 (enero de 1989): 1297–306. http://dx.doi.org/10.1080/02678298908026435.
Texto completoChiellini, E., R. Po, S. Carrozzino, G. Galli y 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, n.º 1 (febrero de 1990): 405–18. http://dx.doi.org/10.1080/00268949008055384.
Texto completoGhanem, 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 (enero de 2007): 117739010700200. http://dx.doi.org/10.4137/117739010700200003.
Texto completoSingh, Nirmal y 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, n.º 8 (18 de junio de 2019): 607–14. http://dx.doi.org/10.2174/1570178616666190123124727.
Texto completoCsuk, René y Anja Kern. "Synthesis of Rigid Cyclopropanoid Nucleoside Analogues". Zeitschrift für Naturforschung B 57, n.º 10 (1 de octubre de 2002): 1169–73. http://dx.doi.org/10.1515/znb-2002-1015.
Texto completoCsuk, René y Gisela Thiede. "Synthesis of Spacered Nucleoside Analogues Comprising a Difluorocyclopropane Moiety". Zeitschrift für Naturforschung B 58, n.º 9 (1 de septiembre de 2003): 853–60. http://dx.doi.org/10.1515/znb-2003-0907.
Texto completoBerthod, Alain, Chau-Dung Chang y Daniel W. Armstrong. "β-Cyclodextrin chiral stationary phases for liquid chromatography. Effect of the spacer arm on chiral recognition". Talanta 40, n.º 9 (septiembre de 1993): 1367–73. http://dx.doi.org/10.1016/0039-9140(93)80212-a.
Texto completoThirunarayanan, Ayyavu y Perumal Rajakumar. "Synthesis, photophysical and electrochemical properties of chiral and achiral thiadiazolophanes". RSC Adv. 4, n.º 45 (2014): 23433–39. http://dx.doi.org/10.1039/c4ra02672a.
Texto completoLiu, Gang, Yukie Saito, Daisuke Nishio-Hamane, Ajoy K. Bauri, Emmanuel Flahaut, Takahide Kimura y Naoki Komatsu. "Structural discrimination of double-walled carbon nanotubes by chiral diporphyrin nanocalipers". J. Mater. Chem. A 2, n.º 44 (2014): 19067–74. http://dx.doi.org/10.1039/c4ta04407j.
Texto completoEma, Tadashi, Shigeharu Misawa, Shuichi Nemugaki, Takashi Sakai y Masanori Utaka. "New Optically Active Diporphyrin Having a Chiral Cyclophane as a Spacer". Chemistry Letters 26, n.º 6 (junio de 1997): 487–88. http://dx.doi.org/10.1246/cl.1997.487.
Texto completoEma, T., S. Misawa, S. Nemugaki, T. Sakai y M. Utaka. "New optically active diporphyrin having a chiral cyclophane as a spacer". Journal of Inorganic Biochemistry 67, n.º 1-4 (julio de 1997): 416. http://dx.doi.org/10.1016/s0162-0134(97)80279-6.
Texto completoPoryvai, Anna, Alexej Bubnov y Michal Kohout. "Chiral Photoresponsive Liquid Crystalline Materials Derived from Cyanoazobenzene Central Core: Effect of UV Light Illumination on Mesomorphic Behavior". Crystals 10, n.º 12 (21 de diciembre de 2020): 1161. http://dx.doi.org/10.3390/cryst10121161.
Texto completoFaye, Valerie, Huu Tinh Nguyen, Valere Law y 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, n.º 1 (agosto de 1997): 183–88. http://dx.doi.org/10.1080/10587259708041765.
Texto completoMizuta, Kenichi, Makoto Katashima, Tomokazu Koga, Kazuhiro Yamabuki, Kenjiro Onimura y Tsutomu Oishi. "Synthesis of chiral side-chain liquid crystalline polyacetylenes bearing succinic acid spacer". Polymer Bulletin 68, n.º 3 (24 de junio de 2011): 623–34. http://dx.doi.org/10.1007/s00289-011-0558-0.
Texto completoWang, Dong, Tian Jun Liu, Chao Jun Li y William T. Slaven. "A chiral conjugated oligomer based on 1,1′-binaphthol with 3,3′-acetylene spacer". Polymer Bulletin 39, n.º 3 (septiembre de 1997): 265–70. http://dx.doi.org/10.1007/s002890050147.
Texto completoStarodubtsev, 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.
Texto completoZhu, Zhao-Xia, Cong-Cong Luo, Ji-Wei Wang, Jian-She Hu y 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, n.º 10 (21 de marzo de 2018): 1525–34. http://dx.doi.org/10.1080/02678292.2018.1453557.
Texto completoWang, Xiaobo, Haohua Li y Ji Zhou. "Asymmetric Transmission in a Mie-Based Dielectric Metamaterial with Fano Resonance". Materials 12, n.º 7 (27 de marzo de 2019): 1003. http://dx.doi.org/10.3390/ma12071003.
Texto completoZhang, Guowen, Man Chao, Shuting Wang, Mengxia Zhu, Dou Wang, Guangsheng Pang y Yanhui Shi. "Synthesis and Catalytic Activity of Chiral Dicarbene Dipalladium Complexes Incorporating the S-binaphthol Unit". Journal of Chemical Research 42, n.º 1 (enero de 2018): 54–56. http://dx.doi.org/10.3184/174751918x15168768395864.
Texto completoJiao, Ti Feng y Jing Xin Zhou. "Chiral Interfacial Assembly of a Trigonal Schiff Base Compound with TPPS in Organized Molecular Films". Applied Mechanics and Materials 236-237 (noviembre de 2012): 810–14. http://dx.doi.org/10.4028/www.scientific.net/amm.236-237.810.
Texto completoHeilmayer, Werner, Bianca Wallfisch, C. Oliver kappe, Curt Wentrup, Karsten Gloe y Gert Kollenz. "Synthesis and Host-abilities of some New Corands Bearing Uncommon Chiral Spacer Units". Supramolecular Chemistry 15, n.º 5 (1 de julio de 2003): 375–83. http://dx.doi.org/10.1080/1061027031000108848.
Texto completoEMA, T., S. MISAWA, S. NEMUGAKI, T. SAKAI y M. UTAKA. "ChemInform Abstract: New Optically Active Diporphyrin Having a Chiral Cyclophane as a Spacer." ChemInform 28, n.º 45 (3 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199745124.
Texto completoRatih, Ratih, Hermann Wätzig, Azminah Azminah, Mufarreh Asmari, Benjamin Peters y 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, n.º 2 (27 de enero de 2021): 98. http://dx.doi.org/10.3390/ph14020098.
Texto completoLi, L. S. y 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, n.º 4 (agosto de 1990): 1100–1101. http://dx.doi.org/10.1017/s042482010017863x.
Texto completoWatanabe, Masami y Kenso Soai. "Enantioselective addition of diethylzinc to aldehydes using chiral polymer catalysts possessing a methylene spacer". Journal of the Chemical Society, Perkin Transactions 1, n.º 7 (1994): 837. http://dx.doi.org/10.1039/p19940000837.
Texto completoLuo, Cong-Cong, Qing-Lin Meng, Ji-Wei Wang, Gui-Yang Yan y Ying-Gang Jia. "Effect of spacer length on mesomorphic behaviours of chiral liquid crystal compounds containing (-)-menthyl". Liquid Crystals 45, n.º 12 (20 de junio de 2018): 1760–70. http://dx.doi.org/10.1080/02678292.2018.1485978.
Texto completoHernández, JoséV, Marta Almaraz, Cesar Raposo, Mercedes Martín, Anna Lithgow, Mercedes Crego, Cruz Caballero y Joaquín R. Morán. "Chiral recognition of tartaric acid derivatives with chromenone-benzoxazole receptors and a spirobifluorene spacer". Tetrahedron Letters 39, n.º 40 (octubre de 1998): 7401–4. http://dx.doi.org/10.1016/s0040-4039(98)01606-2.
Texto completoHirst, Andrew R., David K. Smith, Martin C. Feiters y Huub P. M. Geurts. "Two-Component Dendritic Gel: Effect of Spacer Chain Length on the Supramolecular Chiral Assembly". Langmuir 20, n.º 17 (agosto de 2004): 7070–77. http://dx.doi.org/10.1021/la048751s.
Texto completoYoshizawa, Atsushi, Yukie Soeda y Isa Nishiyama. "Liquid-crystalline properties of a chiral twin material possessing a remarkably flexible central spacer". Journal of Materials Chemistry 5, n.º 4 (1995): 675. http://dx.doi.org/10.1039/jm9950500675.
Texto completoMarcelis, Antonius T. M., Arie Koudijs y Ernst J. R. Sudhölter. "Influence of spacer lengths on the properties of chiral triplet liquid crystals based on estradiol". Liquid Crystals 21, n.º 1 (julio de 1996): 87–93. http://dx.doi.org/10.1080/02678299608033798.
Texto completoShankar, B. Vijai y Archita Patnaik. "Chiral Discrimination of a Gemini-Type Surfactant with Rigid Spacer at the Air−Water Interface". Journal of Physical Chemistry B 111, n.º 39 (octubre de 2007): 11419–27. http://dx.doi.org/10.1021/jp074279i.
Texto completoMiao, Wangen, Dong Yang y Minghua Liu. "Multiple-Stimulus-Responsive Supramolecular Gels and Regulation of Chiral Twists: The Effect of Spacer Length". Chemistry - A European Journal 21, n.º 20 (1 de abril de 2015): 7562–70. http://dx.doi.org/10.1002/chem.201500097.
Texto completoGuldi, Dirk M., Francesco Giacalone, Gema de la Torre, José L. Segura y Nazario Martín. "Topological Effects of a Rigid Chiral Spacer on the Electronic Interactions in Donor–Acceptor Ensembles". Chemistry - A European Journal 11, n.º 24 (9 de diciembre de 2005): 7199–210. http://dx.doi.org/10.1002/chem.200500209.
Texto completoJia, Ying-Gang, Jian-She Hu, Dan Li, Qing-Bao Meng y Xia Zhang. "Synthesis and phase behavior of chiral liquid crystalline polymeric networks derived from menthol". High Performance Polymers 24, n.º 8 (28 de junio de 2012): 673–82. http://dx.doi.org/10.1177/0954008312449843.
Texto completoSeidel, Rüdiger W. y 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, n.º 4 (2 de marzo de 2018): 433–35. http://dx.doi.org/10.1107/s2056989018003055.
Texto completoItoh, Manabu, Masatoshi Tokita, Hiromitsu Hegi, Teruaki Hayakawa, Sungmin Kang y Junji Watanabe. "Enhancement of the cholesteric induction power by macrocyclization in liquid crystal dimers with a chiral spacer". J. Mater. Chem. 21, n.º 6 (2011): 1697–99. http://dx.doi.org/10.1039/c0jm03161e.
Texto completoInaki, Yoshiaki, Shigeki Kamo y Mikiji Miyata. "Base-specific interaction of polymers containing adenine: effect of chiral spacer on the interaction with polynucleotide". Reactive and Functional Polymers 37, n.º 1-3 (junio de 1998): 189–98. http://dx.doi.org/10.1016/s1381-5148(97)00118-1.
Texto completoSoai, Kenso y Masami Watanabe. "New polymer bound chiral catalyst with methylene spacer for the enantioselective addition of diethylzinc to aldehydes". Tetrahedron: Asymmetry 2, n.º 2 (enero de 1991): 97–100. http://dx.doi.org/10.1016/s0957-4166(00)80526-1.
Texto completoWallfisch, Bianca C., Tamara Egger, Werner Heilmayer, C. Oliver Kappe, Curt Wentrup, Karsten Gloe, Ferdinand Belaj, Gerd Klintschar y 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, n.º 5 (1 de julio de 2002): 383–97. http://dx.doi.org/10.1080/1061027021000003430.
Texto completoHo Hyun, Myung y Do Hun Kim. "Spacer length effect of a chiral stationary phase based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid". Chirality 16, n.º 5 (2004): 294–301. http://dx.doi.org/10.1002/chir.20038.
Texto completoWATANABE, M. y K. SOAI. "ChemInform Abstract: Enantioselective Addition of Diethylzinc to Aldehydes Using Chiral Polymer Catalysts Possessing a Methylene Spacer." ChemInform 25, n.º 32 (19 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199432029.
Texto completoAbe, Yunosuke, Toshiki Aoki, Hongge Jia, Shingo Hadano, Takeshi Namikoshi, Yuriko Kakihana, Lijia Liu, Yu Zang, Masahiro Teraguchi y 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, n.º 3 (5 de marzo de 2012): 244–46. http://dx.doi.org/10.1246/cl.2012.244.
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