Статті в журналах з теми "Achiral and chiral"
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Rananaware, Anushri, Duong Duc La, Mohammad Al Kobaisi, Rajesh S. Bhosale, Sidhanath V. Bhosale, and Sheshanath V. Bhosale. "Controlled chiral supramolecular assemblies of water soluble achiral porphyrins induced by chiral counterions." Chemical Communications 52, no. 67 (2016): 10253–56. http://dx.doi.org/10.1039/c6cc04427a.
Повний текст джерелаGuven, Zekiye P., Burcin Ustbas, Kellen M. Harkness, Hikmet Coskun, Chakra P. Joshi, Tabot M. D. Besong, Francesco Stellacci, Osman M. Bakr, and Ozge Akbulut. "Synthesis and characterization of mixed ligand chiral nanoclusters." Dalton Transactions 45, no. 28 (2016): 11297–300. http://dx.doi.org/10.1039/c6dt00785f.
Повний текст джерелаReyes Calle, Juliana, Jairo Antonio Cubillos Lobo, Consuelo Montes de Correa, and Aída Luz Villa Holguín de P. "Oxidising agent and catalyst chirality effect on epoxidation of R-(+)- Limonene using Jacobsen-type catalysts." Ingeniería e Investigación 28, no. 2 (May 1, 2008): 37–44. http://dx.doi.org/10.15446/ing.investig.v28n2.14890.
Повний текст джерелаPakalidou, Nikoletta, David L. Cheung, Andrew J. Masters, and Carlos Avendaño. "Macroscopic chiral symmetry breaking in monolayers of achiral nonconvex platelets." Soft Matter 13, no. 45 (2017): 8618–24. http://dx.doi.org/10.1039/c7sm01840a.
Повний текст джерелаWilson, Tyler M., Audra Davis, Reilly E. Sonstrom, Justin L. Neill, Emma A. Ziebarth, Ariel Poulson, and Richard E. Carlson. "Essential Oil Composition and Enantioselective Profile of Agastache urticifolia (Lamiaceae) and Monardella odoratissima (Lamiaceae) from Utah." Molecules 28, no. 5 (February 28, 2023): 2249. http://dx.doi.org/10.3390/molecules28052249.
Повний текст джерелаWang, Lewen, Tengfei He, Hailiang Liao, Yige Luo, Wen Ou, Yinye Yu, Wan Yue, Guankui Long, Xingzhan Wei, and Yecheng Zhou. "A Theoretical Design of Chiral Molecules through Conformational Lock towards Circularly Polarized Luminescence." Photonics 9, no. 8 (July 29, 2022): 532. http://dx.doi.org/10.3390/photonics9080532.
Повний текст джерелаDressel, Christian, Wolfgang Weissflog, and Carsten Tschierske. "Spontaneous mirror symmetry breaking in a re-entrant isotropic liquid." Chemical Communications 51, no. 87 (2015): 15850–53. http://dx.doi.org/10.1039/c5cc06843f.
Повний текст джерелаBecalski, Adam, William R. Cullen, Michael D. Fryzuk, Georg Herb, Brian R. James, James P. Kutney, Krystyna Piotrowska, and Dianne Tapiolas. "The chemistry of thujone. XII. The synthesis of pyrethroid analogues via chiral cyclopropanation." Canadian Journal of Chemistry 66, no. 12 (December 1, 1988): 3108–15. http://dx.doi.org/10.1139/v88-479.
Повний текст джерелаDestoop, Iris, Andrea Minoia, Oleksandr Ivasenko, Aya Noguchi, Kazukuni Tahara, Yoshito Tobe, Roberto Lazzaroni, and Steven De Feyter. "Transfer of chiral information from a chiral solvent to a two-dimensional network." Faraday Discussions 204 (2017): 215–31. http://dx.doi.org/10.1039/c7fd00103g.
Повний текст джерелаJin, Lei, Xiongyu Liang, Chengmao He, Tiejun Wang, Kun Liang, and Li Yu. "Plasmon—Assisted Resonance Energy Transfer Involving Electric and Magnetic Coupling." Electronics 13, no. 8 (April 19, 2024): 1566. http://dx.doi.org/10.3390/electronics13081566.
Повний текст джерелаLee, Yen, Boyeong Kang, and Jiwon Seo. "Metalloporphyrin Dimers Bridged by a Peptoid Helix: Host-Guest Interaction and Chiral Recognition." Molecules 23, no. 11 (October 24, 2018): 2741. http://dx.doi.org/10.3390/molecules23112741.
Повний текст джерелаZhang, Wanning, Hui Chang, Jing Ai, Shunai Che, Yingying Duan, and Lu Han. "Spontaneous chiral self-assembly of achiral AIEgens into AIEgen-silica hybrid nanotubes." Chemical Communications 55, no. 96 (2019): 14438–41. http://dx.doi.org/10.1039/c9cc06873b.
Повний текст джерелаTanaka, Koichi, Takaichi Hiratsuka, Yuko Kojima, and Yasuko T. Osano. "Synthesis, Structure and Chiral Inclusion Crystallisation of Tetrakis(4-Ethynylphenyl)Ethylene Derivatives." Journal of Chemical Research 2002, no. 5 (May 2002): 209–12. http://dx.doi.org/10.3184/030823402103171889.
Повний текст джерелаMemmer, Reiner, and Folkert Janssen. "Computer Simulation of Chiral Liquid Crystal Phases IX. Chiral Induction in Guest-host Systems - Calculation of the Helical Twisting Power." Zeitschrift für Naturforschung A 54, no. 12 (December 1, 1999): 747–54. http://dx.doi.org/10.1515/zna-1999-1212.
Повний текст джерелаLiu, Yiyi, Tharaka Perera, Qianqian Shi, Zijun Yong, Sudaraka Mallawaarachchi, Bo Fan, Julia Ann-Therese Walker, et al. "Thermoresponsive chiral plasmonic nanoparticles." Nanoscale 14, no. 11 (2022): 4292–303. http://dx.doi.org/10.1039/d1nr08343k.
Повний текст джерелаRoyes, Jorge, Víctor Polo, Santiago Uriel, Luis Oriol, Milagros Piñol, and Rosa M. Tejedor. "Chiral supramolecular organization from a sheet-like achiral gel: a study of chiral photoinduction." Physical Chemistry Chemical Physics 19, no. 21 (2017): 13622–28. http://dx.doi.org/10.1039/c7cp01739a.
Повний текст джерелаZhang, Yingjie, and Jianping Deng. "Chiral helical polymer materials derived from achiral monomers and their chiral applications." Polymer Chemistry 11, no. 34 (2020): 5407–23. http://dx.doi.org/10.1039/d0py00934b.
Повний текст джерелаAlexandrov, Anatoly I., and Tamara V. Pashkova. "Structure Investigation of Mesogenic Homo- and Copolymers Based on Chiral and Achiral Acrylates." Liquid Crystals and their Application 23, no. 4 (December 26, 2023): 82–93. http://dx.doi.org/10.18083/lcappl.2023.4.82.
Повний текст джерелаMislow, Kurt. "Absolute Asymmetric Synthesis: A Commentary." Collection of Czechoslovak Chemical Communications 68, no. 5 (2003): 849–64. http://dx.doi.org/10.1135/cccc20030849.
Повний текст джерелаWang, Chao, Hua Hao, Daisuke Hashizume, and Keisuke Tajima. "Surface-induced enantiomorphic crystallization of achiral fullerene derivatives in thin films." Chemical Science 11, no. 18 (2020): 4702–8. http://dx.doi.org/10.1039/d0sc01163k.
Повний текст джерелаMiao, Tengfei, Xiaoxiao Cheng, Haotian Ma, Wei Zhang, and Xiulin Zhu. "Induction, fixation and recovery of self-organized helical superstructures in achiral liquid crystalline polymer." Polymer Chemistry 12, no. 41 (2021): 5931–36. http://dx.doi.org/10.1039/d1py01206a.
Повний текст джерелаWang, Xiongbin, Junjie Hao, Jiaji Cheng, Junzi Li, Jun Miao, Ruxue Li, Yiwen Li, et al. "Chiral CdSe nanoplatelets as an ultrasensitive probe for lead ion sensing." Nanoscale 11, no. 19 (2019): 9327–34. http://dx.doi.org/10.1039/c8nr10506e.
Повний текст джерелаPark, Changjun, Jinhee Lee, Taehyoung Kim, Jaechang Lim, Jeyoung Park, Woo Youn Kim, and Sang Youl Kim. "Homochiral Supramolecular Thin Film from Self-Assembly of Achiral Triarylamine Molecules by Circularly Polarized Light." Molecules 25, no. 2 (January 18, 2020): 402. http://dx.doi.org/10.3390/molecules25020402.
Повний текст джерелаLi, Wenfang, Zeyuan Dong, Junyan Zhu, Quan Luo, and Junqiu Liu. "Spontaneous formation of organic helical architectures through dynamic covalent chemistry." Chem. Commun. 50, no. 94 (2014): 14744–47. http://dx.doi.org/10.1039/c4cc07263d.
Повний текст джерелаRamamurthy. "Achiral Zeolites as Reaction Media for Chiral Photochemistry." Molecules 24, no. 19 (October 2, 2019): 3570. http://dx.doi.org/10.3390/molecules24193570.
Повний текст джерелаŠtěpánek, Petr, Ondřej Vích, Lukáš Werner, Ladislav Kniežo, Hana Dvořáková та Pavel Vojtíšek. "Stereoselective Preparation of Precursors of α-C-(1→3)-Disaccharides". Collection of Czechoslovak Chemical Communications 70, № 9 (2005): 1411–28. http://dx.doi.org/10.1135/cccc20051411.
Повний текст джерелаMU, WEIHUA, ANTHONY NICKOLAS VAMIVAKAS, YAN FANG, and BOLIN WANG. "PHONON DISPERSION IN CHIRAL SINGLE-WALL CARBON NANOTUBES." Modern Physics Letters B 21, no. 25 (October 30, 2007): 1667–76. http://dx.doi.org/10.1142/s021798490701419x.
Повний текст джерелаImai, Yoshitane. "Generation of Circularly Polarized Luminescence by Symmetry Breaking." Symmetry 12, no. 11 (October 28, 2020): 1786. http://dx.doi.org/10.3390/sym12111786.
Повний текст джерелаRusková, Renáta, and Dušan Račko. "Knot Formation on DNA Pushed Inside Chiral Nanochannels." Polymers 15, no. 20 (October 22, 2023): 4185. http://dx.doi.org/10.3390/polym15204185.
Повний текст джерелаLi, Hanbo, Xinshuang Gao, Chenqi Zhang, Yinglu Ji, Zhijian Hu, and Xiaochun Wu. "Gold-Nanoparticle-Based Chiral Plasmonic Nanostructures and Their Biomedical Applications." Biosensors 12, no. 11 (November 1, 2022): 957. http://dx.doi.org/10.3390/bios12110957.
Повний текст джерелаLee, Jae-Jin, and Suk-Won Choi. "Preferential Circularly Polarized Luminescence from a Nano-Segregated Liquid Crystalline Phase Using a Polymerized Twisted Nematic Platform." Polymers 12, no. 11 (October 29, 2020): 2529. http://dx.doi.org/10.3390/polym12112529.
Повний текст джерелаLee, Hyoung-In. "Spin–Orbital Coupling and Conservation Laws in Electromagnetic Waves Propagating through Chiral Media." Optics 4, no. 1 (January 18, 2023): 100–131. http://dx.doi.org/10.3390/opt4010008.
Повний текст джерелаFu, Jingke, Xiaohong Huo, Bowen Li, and Wanbin Zhang. "Cooperative bimetallic catalysis in asymmetric allylic substitution." Organic & Biomolecular Chemistry 15, no. 46 (2017): 9747–59. http://dx.doi.org/10.1039/c7ob02476b.
Повний текст джерелаZhang, Qingfeng, Taylor Hernandez, Kyle W. Smith, Seyyed Ali Hosseini Jebeli, Alan X. Dai, Lauren Warning, Rashad Baiyasi, et al. "Unraveling the origin of chirality from plasmonic nanoparticle-protein complexes." Science 365, no. 6460 (September 26, 2019): 1475–78. http://dx.doi.org/10.1126/science.aax5415.
Повний текст джерелаHarris, Robert A. "Chiral fluctuations in achiral systems." Journal of Chemical Physics 115, no. 23 (December 15, 2001): 10577–80. http://dx.doi.org/10.1063/1.1427024.
Повний текст джерелаSTINSON, STEPHEN. "Achiral ligands abet chiral catalysis." Chemical & Engineering News 78, no. 10 (March 6, 2000): 14. http://dx.doi.org/10.1021/cen-v078n010.p014.
Повний текст джерелаFlack, Howard D. "Chiral and Achiral Crystal Structures." Helvetica Chimica Acta 86, no. 4 (April 2003): 905–21. http://dx.doi.org/10.1002/hlca.200390109.
Повний текст джерелаGeng, Bin, Ling-Xiang Guo, Bao-Ping Lin, Patrick Keller, Xue-Qin Zhang, Ying Sun, and Hong Yang. "Side chain liquid crystalline polymers with an optically active polynorbornene backbone and achiral mesogenic side groups." Polymer Chemistry 6, no. 29 (2015): 5281–87. http://dx.doi.org/10.1039/c5py00651a.
Повний текст джерелаReddy, Kumbam Lingeshwar, Jikson Pulparayil Mathew, Sonia Maniappan, Catherine Tom, Elizabeth Shiby, Ravi Kumar Pujala, and Jatish Kumar. "Mandelic acid appended chiral gels as efficient templates for multicolour circularly polarized luminescence." Nanoscale 14, no. 13 (2022): 4946–56. http://dx.doi.org/10.1039/d1nr08506a.
Повний текст джерелаFernández, Zulema, Berta Fernández, Emilio Quiñoá, Ricardo Riguera, and Félix Freire. "Chiral information harvesting in helical poly(acetylene) derivatives using oligo(p-phenyleneethynylene)s as spacers." Chemical Science 11, no. 27 (2020): 7182–87. http://dx.doi.org/10.1039/d0sc02685a.
Повний текст джерелаMou, Qi, Ruyuan Zhao, Ruihan Niu, Seiya Fukagawa, Taiki Shigeno, Tatsuhiko Yoshino, Shigeki Matsunaga, and Bo Sun. "Cp*Ir(iii)/chiral carboxylic acid-catalyzed enantioselective C–H alkylation of ferrocene carboxamides with diazomalonates." Organic Chemistry Frontiers 8, no. 24 (2021): 6923–30. http://dx.doi.org/10.1039/d1qo01344k.
Повний текст джерелаZinna, Francesco, Lorenzo Arrico, Tiziana Funaioli, Lorenzo Di Bari, Mariacecilia Pasini, Chiara Botta, and Umberto Giovanella. "Modular chiral Eu(iii) complexes for efficient circularly polarized OLEDs." Journal of Materials Chemistry C 10, no. 2 (2022): 463–68. http://dx.doi.org/10.1039/d1tc05023k.
Повний текст джерелаHan, Yun-Hu, Yue-Cheng Liu, Xiu-Shuang Xing, Chong-Bin Tian, Ping Lin, and Shao-Wu Du. "Chiral template induced homochiral MOFs built from achiral components: SHG enhancement and enantioselective sensing of chiral alkamines by ion-exchange." Chemical Communications 51, no. 77 (2015): 14481–84. http://dx.doi.org/10.1039/c5cc05566k.
Повний текст джерелаPan, Chongqing, Si-Yong Yin, Qing Gu, and Shu-Li You. "CpxM(iii)-catalyzed enantioselective C–H functionalization through migratory insertion of metal–carbenes/nitrenes." Organic & Biomolecular Chemistry 19, no. 34 (2021): 7264–75. http://dx.doi.org/10.1039/d1ob01248g.
Повний текст джерелаSchuette, Jodi M., A. Yvette Will, Rezik A. Agbaria, and Isiah M. Warner. "Fluorescence Characterization of the Cyclodextrin/Pyrene Complex Interaction with Chiral Alcohols and Diols." Applied Spectroscopy 48, no. 5 (May 1994): 581–86. http://dx.doi.org/10.1366/0003702944924934.
Повний текст джерелаGuerrero, M. M. López, A. Navas Díaz, F. García Sánchez, and H. Corrall. "Chiral and Achiral Enantiomeric Separation of (±)-Alprenolol." Open Chemistry 17, no. 1 (June 12, 2019): 429–37. http://dx.doi.org/10.1515/chem-2019-0049.
Повний текст джерелаKrekic, Szilvia, Mark Mero, Michel Kuhl, Kannan Balasubramanian, András Dér, and Zsuzsanna Heiner. "Photoactive Yellow Protein Adsorption at Hydrated Polyethyleneimine and Poly-l-Glutamic Acid Interfaces." Molecules 28, no. 10 (May 13, 2023): 4077. http://dx.doi.org/10.3390/molecules28104077.
Повний текст джерелаWang, Juan, Zhen Wei, Fengwan Guo, Chenyang Li, Pengfei Zhu, and Wenhua Zhu. "Homochiral 3D coordination polymer with unprecedented three-directional helical topology from achiral precursor: synthesis, crystal structure, and luminescence properties of uranyl succinate metal–organic framework." Dalton Transactions 44, no. 31 (2015): 13809–13. http://dx.doi.org/10.1039/c5dt02111a.
Повний текст джерелаKatoono, Ryo, Keiichi Kusaka, Yuki Saito, Kazuki Sakamoto, and Takanori Suzuki. "Chiral diversification through the assembly of achiral phenylacetylene macrocycles with a two-fold bridge." Chemical Science 10, no. 18 (2019): 4782–91. http://dx.doi.org/10.1039/c9sc00972h.
Повний текст джерелаCarballo, Rosa, Alfonso Castiñeiras, Berta Covelo, Ana B. Lago, Ezequiel M. Vázquez-López, Olaya Gómez-Paz, Susana Balboa, and Inmaculada Prieto. "Chiral and achiral 1D copper(ii) coordination polymers based on glycolato and chelating aromatic diamine ligands." CrystEngComm 20, no. 17 (2018): 2455–64. http://dx.doi.org/10.1039/c8ce00279g.
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