Relevant bibliographies by topics / Porosity. Crystal growth. Supramolecular chemistry

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters

Academic literature on the topic 'Porosity. Crystal growth. Supramolecular chemistry'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Porosity. Crystal growth. Supramolecular chemistry"

1

Hyodo, Tadashi, Masahide Tominaga, and Kentaro Yamaguchi. "Guest-dependent single-crystal-to-single-crystal transformations in porous adamantane-bearing macrocycles." CrystEngComm 23, no. 7 (2021): 1539–43. http://dx.doi.org/10.1039/d0ce01782e.

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An adamantane-bearing macrocycle exhibited permanent intrinsic porosity and adsorption of small guests in single-crystal-to-single-crystal fashions. The guest capture resulted in the structural transformations of supramolecular organic frameworks.
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Chong, Samantha, Tom Hasell, Jamie Culshaw, et al. "Exploiting weak supramolecular interactions to assemble organic cage materials." Acta Crystallographica Section A Foundations and Advances 70, a1 (2014): C632. http://dx.doi.org/10.1107/s205327331409367x.

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Intensive research into microporous materials has been driven by potential applications in areas such as catalysis, gas separation, storage, and sensing. Recently, a new class of purely organic molecular cage materials has emerged, which can exhibit significant porosity arising from the internal molecular cavity as well as extrinsic porosity from packing in the crystal structure [1]. Unlike extended frameworks, porous molecular materials lack strongly directional interactions to drive their assembly, complicating the crystal engineering possible for isoreticular metal-organic frameworks [2], f
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3

Foster, Jonathan A., Marc-Oliver M. Piepenbrock, Gareth O. Lloyd, Nigel Clarke, Judith A. K. Howard, and Jonathan W. Steed. "Anion-switchable supramolecular gels for controlling pharmaceutical crystal growth." Nature Chemistry 2, no. 12 (2010): 1037–43. http://dx.doi.org/10.1038/nchem.859.

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4

Epishin, Alexander, Thomas Link, Igor Leonidovich Svetlov, Gert Nolze, Romeo Saliwan Neumann, and Henning Lucas. "Mechanism of porosity growth during homogenisation in single crystal nickel-based superalloys." International Journal of Materials Research 104, no. 8 (2013): 776–82. http://dx.doi.org/10.3139/146.110924.

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5

Serdobintseva, V. V., D. V. Kalinin, A. F. Danilyuk, and N. A. Rudina. "Supramolecular crystal growth in concentrated suspensions of charged monodisperse spherical silica particles." Reaction Kinetics and Catalysis Letters 68, no. 2 (1999): 313–18. http://dx.doi.org/10.1007/bf02475518.

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6

Li, Hang, Fanchen Meng, Suoying Zhang, et al. "Crystal‐Growth‐Dominated Fabrication of Metal–Organic Frameworks with Orderly Distributed Hierarchical Porosity." Angewandte Chemie International Edition 59, no. 6 (2020): 2457–64. http://dx.doi.org/10.1002/anie.201912972.

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7

Shin, Jong Won, Ah Rim Jeong, Younghak Kim, et al. "Solvent-triggered single-crystal-to-single-crystal transformation from a monomeric to polymeric copper(II) complex based on an aza macrocyclic ligand." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 76, no. 2 (2020): 225–32. http://dx.doi.org/10.1107/s2052520620002371.

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Reversible solvent-triggered single-crystal-to-single-crystal (SCSC) transformations are observed between two copper(II) azamacrocyclic complexes: [Cu(C16H38N6)(H2O)2](C12H6O4) (1) and [Cu(C16H38N6)(C12H6O4)] (2). Complex (1) was prepared via self-assembly of a copper(II) azamacrocyclic complex containing butyl pendant groups, [Cu(C16H38N6)(ClO4)2], with 2,7-naphthalenedicarboxylic acid. When monomeric compound (1) was immersed in CH3OH, coordination polymer (2) was obtained, indicating a solvent-triggered SCSC transformation. Furthermore, when (2) was immersed in water, an reverse SCSC transf
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Thomas, Jency, and Arunachalam Ramanan. "Growth of Copper Pyrazole Complex Templated Phosphomolybdates: Supramolecular Interactions Dictate Nucleation of a Crystal." Crystal Growth & Design 8, no. 9 (2008): 3390–400. http://dx.doi.org/10.1021/cg800344h.

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9

Lini, Freshsya Zata, Dhanang Edy Pratama, and Tu Lee. "Co-Crystallization Kinetics of 2:1 Benzoic Acid–Sodium Benzoate Co-Crystal: The Effect of Templating Molecules in a Solution." Crystals 11, no. 7 (2021): 812. http://dx.doi.org/10.3390/cryst11070812.

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The addition of dissolved templating molecules in crystallization will create “supramolecular assemblies” within the solution, serving as “anchor points” for the solute molecules to nucleate and grow. In this work, nucleation and crystal growth kinetics of 2:1 benzoic acid (HBz)–sodium benzoate (NaBz) co-crystallization with or without templates in a solution were analyzed by monitoring the concentration of the mother liquor during cooling crystallization. The results showed that the addition of the dissolved 2:1 or 1:1 HBz–NaBz co-crystals as templating molecules could reduce the critical fre
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10

LIU, Xi, Bo-Yuan CHEN, Zhi-Zhan CHEN, Li-Xin SONG, and Er-Wei SHI. "Effects of the Porosity of the Source Materials on the Initial Growth of 6H-SiC Crystal." Journal of Inorganic Materials 25, no. 2 (2010): 177–80. http://dx.doi.org/10.3724/sp.j.1077.2010.00177.

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Dissertations / Theses on the topic "Porosity. Crystal growth. Supramolecular chemistry"

1

Lloyd, Gareth Owen. "Crystal engineering of porosity." Thesis, Link to the online version, 2006. http://hdl.handle.net/10019/1087.

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Wahl, Helene. "Development of novel supramolecular framework materials based on organic salts." Thesis, Stellenbosch : Stellenbosch University, 2014. http://hdl.handle.net/10019.1/95858.

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Thesis (PhD)--Stellenbosch University, 2014.<br>ENGLISH ABSTRACT: The aim of the work presented in this thesis was to design ionic organic framework materials based on carboxylate salts with the intention of engineering interesting properties, such as porosity, into these framework materials. The first section focuses on the characterisation and porosity studies of an ionic framework material, 3,4-lutidinium pamoate hemihydrate, with THF-filled channels in the solid state. It was shown that this framework is able to exchange the THF in the channels for a wide variety of compounds, with many o
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3

Rather, Elisabeth. "Supramolecular metal-organic and organic materials." [Tampa, Fla.] : University of South Florida, 2004. http://purl.fcla.edu/fcla/etd/SFE0000267.

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Adolf, Cyril. "Cristaux moléculaires : des cristaux coeur-coquille aux réseaux de cristaux." Thesis, Strasbourg, 2017. http://www.theses.fr/2017STRAF026/document.

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L’agencement relatif de systèmes cristallins moléculaires, par une méthode d’organisation avancée est une stratégie de premier plan. Le développement de tels systèmes permet la conception de dispositifs innovants dans le domaine des matériaux poreux, magnétiques ou optiques.Les travaux menés dans le cadre de cette étude ont pour objectif l’élaboration d’architectures macroscopiques hiérarchisées concernant l’état cristallin, de type « réseaux de cristaux ». Dans un premier temps, le développement et la caractérisation de réseaux iso-structuraux ont été réalisés. Ces séries, formées par liaison
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Blair-Pereira, Joao-Nicolas. "Tectonique moléculaire : vers l'utilisation du dispirofluorène-indénofluorène comme unité de construction pour bâtir des réseaux cristallins poreux." Thèse, 2013. http://hdl.handle.net/1866/9817.

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La chimie supramoléculaire est un domaine qui suscite depuis quelques années un intérêt grandissant. Le domaine s’appuie sur les interactions intermoléculaires de façon à contrôler l’organisation moléculaire et ainsi moduler les propriétés des matériaux. La sélection et le positionnement adéquat de groupes fonctionnels, utilisés en combinaison avec un squelette moléculaire particulier, permet d’anticiper la façon dont une molécule interagira avec les molécules avoisinantes. Cette stratégie de construction, nommé tectonique moléculaire, fait appel à la conception de molécules appelées tecton
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Books on the topic "Porosity. Crystal growth. Supramolecular chemistry"

1

The importance of Pi-interactions in crystal engineering: Frontiers in crystal engineering. Wiley, 2012.

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2

Tiekink, Edward R. T., and Julio Zukerman-Schpector. Importance of Pi-Interactions in Crystal Engineering: Frontiers in Crystal Engineering. Wiley & Sons, Incorporated, John, 2012.

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Tiekink, Edward R. T., and Julio Zukerman-Schpector. Importance of Pi-Interactions in Crystal Engineering: Frontiers in Crystal Engineering. Wiley & Sons, Limited, John, 2012.

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Tiekink, Edward R. T., and Julio Zukerman-Schpector. Importance of Pi-Interactions in Crystal Engineering: Frontiers in Crystal Engineering. Wiley & Sons, Incorporated, John, 2012.

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Tiekink, Edward R. T., and Julio Zukerman-Schpector. Importance of Pi-Interactions in Crystal Engineering: Frontiers in Crystal Engineering. Wiley & Sons, Incorporated, John, 2012.

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Book chapters on the topic "Porosity. Crystal growth. Supramolecular chemistry"

1

Blagden, Nicholas. "Crystal Growth Mechanisms." In Encyclopedia of Supramolecular Chemistry. CRC Press, 2004. http://dx.doi.org/10.1081/e-esmc-120012753.

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Journal articles
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