Bibliografias temáticas / Pillar[n]arene

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Literatura científica selecionada sobre o tema "Pillar[n]arene"

Autor: Grafiati

Publicado: 1 de abril de 2023

Última modificação: 25 de julho de 2025

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Artigos de revistas sobre o assunto "Pillar[n]arene"

Xie, Changdong, Weibo Hu, Wenjing Hu, et al. "Synthesis of Pillar[n]arene[5−n]quininesviaPartial Oxidation of Pillar[5]arene." Chinese Journal of Chemistry 33, no. 3 (2015): 379–83. http://dx.doi.org/10.1002/cjoc.201400895.

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Liu, Zhaona, Bing Li, Zhizheng Li, and Huacheng Zhang. "Pillar[n]arene-Mimicking/Assisted/Participated Carbon Nanotube Materials." Materials 15, no. 17 (2022): 6119. http://dx.doi.org/10.3390/ma15176119.

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The recent progress in pillar[n]arene-assisted/participated carbon nanotube hybrid materials were initially summarized and discussed. The molecular structure of pillar[n]arene could serve different roles in the fabrication of attractive carbon nanotube-based materials. Firstly, pillar[n]arene has the ability to provide the structural basis for enlarging the cylindrical pillar-like architecture by forming one-dimensional, rigid, tubular, oligomeric/polymeric structures with aromatic moieties as the linker, or forming spatially “closed”, channel-like, flexible structures by perfunctionalizing wi

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Li, Xu, Yan Jin, Nansong Zhu, and Long Yi Jin. "Applications of Supramolecular Polymers Generated from Pillar[n]arene-Based Molecules." Polymers 15, no. 23 (2023): 4543. http://dx.doi.org/10.3390/polym15234543.

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Supramolecular chemistry enables the manipulation of functional components on a molecular scale, facilitating a “bottom-up” approach to govern the sizes and structures of supramolecular materials. Using dynamic non-covalent interactions, supramolecular polymers can create materials with reversible and degradable characteristics and the abilities to self-heal and respond to external stimuli. Pillar[n]arene represents a novel class of macrocyclic hosts, emerging after cyclodextrins, crown ethers, calixarenes, and cucurbiturils. Its significance lies in its distinctive structure, comparing an ele

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Liu, Zhaona, Zhizheng Li, Bing Li, Le Zhou, Huacheng Zhang, and Jie Han. "Hybrid Macrocyclic Polymers: Self-Assembly Containing Cucurbit[m]uril-pillar[n]arene." Polymers 14, no. 9 (2022): 1777. http://dx.doi.org/10.3390/polym14091777.

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Supramolecular self-assembly by hybrid macrocycles containing both cucurbit[m]uril (CB[m]) and pillar[n]arene was discussed and summarized in this review. Due to different solubility, diverse-sized cavities, and various driving forces in recognizing guests, the role of CB[m] and pillar[n]arene in such hybrid macrocyclic systems could switch between competitor in capturing specialized guests, and cooperator for building advanced hybridized macrocycles, by controlling their characteristics in host–guest inclusions. Furthermore, both CB[m] and pillar[n]arene were employed for fabricating advanced

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Gorbachuk, Vladimir V., Anna R. Marysheva, and Ivan I. Stoykov. "Total oxidation of decahydroxypillar[5]arene with copper(II) and iron(III) nitrates." Butlerov Communications 63, no. 7 (2020): 19–23. http://dx.doi.org/10.37952/roi-jbc-01/20-63-7-19.

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Pillar[n]arenes are suitable synthetic platforms for synthesis of functionalized p-cyclophanes, versatile building blocks for creating supramolecular polymers and (pseudo)rotaxanes. The presence of hydroquinone fragments in unsubstituted pillar[n]arene derivatives opens wide opportunities for their application in electrochemical sensors and for their use as reducing agents for synthesis of hybrid materials. Macrocyclic cavity plays the key role in molecular recognition, supramolecular self-assembly of pillararenes, and therefore possibility of switching electron donor properties of aromatic mo

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Zuilhof, Han, Andrew C.-H. Sue, and Jorge Escorihuela. "On the Stability and Formation of Pillar[n]arenes: a DFT Study." Journal of Organic Chemistry 86, no. 21 (2021): 14956–63. https://doi.org/10.1021/acs.joc.1c01679.

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The increased use of both pillar[5]arenes and pillar[6]arenes, stimulated by increasingly efficient syntheses of both, has brought forward the question as to what drives the intermediates in this Friedel–Crafts ring formation to form a pillar[5]arene, a pillar[6]arene, or any other sized macrocycle. This study sets out to answer this question by studying both the thermodynamics and kinetics involved in the absence and presence of templating solvents using high-end wB97XD/6-311G(2p,2d) DFT calculations.

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Liu, Zhaona, Bing Li, Leqian Song, and Huacheng Zhang. "Pillar[n]arene–calix[m]arene hybrid macrocyclic structures." RSC Advances 12, no. 43 (2022): 28185–95. http://dx.doi.org/10.1039/d2ra05118d.

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Khalil-Cruz, Laila E., Peiren Liu, Feihe Huang, and Niveen M. Khashab. "Multifunctional Pillar[n]arene-Based Smart Nanomaterials." ACS Applied Materials & Interfaces 13, no. 27 (2021): 31337–54. http://dx.doi.org/10.1021/acsami.1c05798.

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Zhang, Huacheng, Zhaono Liu, Feifei Xin, and Aaiyou Hao. "Synthesis and Application of Pillar[n]arene." Chinese Journal of Organic Chemistry 32, no. 2 (2012): 219. http://dx.doi.org/10.6023/cjoc1107141.

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Xu, Xiaowen, Valentin Victor Jerca, and Richard Hoogenboom. "Structural Diversification of Pillar[ n ]arene Macrocycles." Angewandte Chemie International Edition 59, no. 16 (2020): 6314–16. http://dx.doi.org/10.1002/anie.202002467.

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Mais fontes

Teses / dissertações sobre o assunto "Pillar[n]arene"

DA, PIAN MARTA. "Synthesis, Mechanism and Catalytic Applications of Pillar[n]arenes." Doctoral thesis, Università degli Studi di Trieste, 2018. http://hdl.handle.net/11368/2920043.

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Pillar[n]arenes (P[n] n = 5-15) are a new class of macrocyclic arenes discovered for the first time by Ogoshi in 2008, which attracted a lot of attention due to their unique binding properties towards neutral electron poor compounds. Our research was focused on the enhancement of the yield of the larger macrocycle P[6], starting from three different alkoxy substituted benzene derivatives. Our synthetic approach involved the study of a series of small organic and organometallic cations in the role of a template, such as a cobaltocenium salt, ferrocenium salt, tetramethylammonium chloride and bu

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