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Journal articles on the topic 'Supramolecular organic chemistry'

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Author: Grafiati

Published: 10 December 2022

Last updated: 28 January 2023

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1

Sherburn, Michael. "Introduction to Supramolecular Chemistry By Helena Dodziuk." Australian Journal of Chemistry 55, no. 5 (2002): 357. http://dx.doi.org/10.1071/ch02004_br.

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Introduction to Supramolecular ChemistryBy Helena DodziukKluwer Academic Publishers, The Netherlands.December 2001, 364 pp.ISBN 1402002149Hardcover, 82.00 GBP.Introduction to Supramolecular Chemistry by Dr Helena Dodziuk of the Institute of Physical Chemistry, Polish Academy of Sciences, is a broad summary of chemical aspects of supramolecular science. * Dr Michael Sherburn is a senior lecturer in organic chemistry at the School of Chemistry, the University of Sydney.

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2

Bose, Anima, and Prasenjit Mal. "Mechanochemistry of supramolecules." Beilstein Journal of Organic Chemistry 15 (April 12, 2019): 881–900. http://dx.doi.org/10.3762/bjoc.15.86.

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The urge to use alternative energy sources has gained significant attention in the eye of chemists in recent years. Solution-based traditional syntheses are extremely useful, although they are often associated with certain disadvantages like generation of waste as by-products, use of large quantities of solvents which causes environmental hazard, etc. Contrastingly, achieving syntheses through mechanochemical methods are generally time-saving, environmentally friendly and more economical. This review is written to shed some light on supramolecular chemistry and the synthesis of various supramolecules through mechanochemistry.

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3

Hr. "Supramolecular Chemistry." Journal of Molecular Structure 274 (November 1992): 315. http://dx.doi.org/10.1016/0022-2860(92)80171-d.

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4

Serpe, Michael J., and Stephen L. Craig. "Physical Organic Chemistry of Supramolecular Polymers." Langmuir 23, no. 4 (February 2007): 1626–34. http://dx.doi.org/10.1021/la0621416.

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5

Gasparini, Giulio, Eun-Kyoung Bang, Javier Montenegro, and Stefan Matile. "Cellular uptake: lessons from supramolecular organic chemistry." Chemical Communications 51, no. 52 (2015): 10389–402. http://dx.doi.org/10.1039/c5cc03472h.

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6

Jolliffe, Katrina (Kate) A., and Philip A. Gale. "The supramolecular chemistry of anions." Organic & Biomolecular Chemistry 20, no. 4 (2022): 713–14. http://dx.doi.org/10.1039/d1ob90183d.

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7

Haino, Takeharu, Ryo Sekiya, Kentaro Harada, and Natsumi Nitta. "Resorcinarene-Based Supramolecular Capsules: Supramolecular Functions and Applications." Synlett 33, no. 06 (October 27, 2021): 518–30. http://dx.doi.org/10.1055/a-1679-8141.

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AbstractA resorcinarene is a synthetic macrocycle consisting of four resorcinol molecules covalently linked by methylene bridges. The interannular bridges produce a cavitand that has a bowl-shaped structure. We have developed supramolecular capsules through Ag(I) or Cu(I) coordination-driven self-assembly of cavitands possessing 2,2′-bipyridyl arms in their upper rims. The self-assembled capsules accommodate various molecular guests and supramolecular assemblies possessing acetoxy groups. The host–guest chemistry of the molecular capsules has been applied in the fabrication of supramolecular polymers. This account describes recent developments in the supramolecular chemistry of resorcinarene-based coordination capsules and provides a brief history of resorcinarene-based capsules and related capsules.

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8

Saji, Viswanathan S. "Supramolecular concepts and approaches in corrosion and biofouling prevention." Corrosion Reviews 37, no. 3 (June 26, 2019): 187–230. http://dx.doi.org/10.1515/corrrev-2018-0105.

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AbstractSupramolecular chemistry is one of the exciting branches of chemistry where non-covalent interactions between molecules and the ensuing supramolecular structures have been studied for various applications. The present review provides a comprehensive outlook on the applications and potentials of supramolecular chemistry in corrosion and biofouling prevention. Reported works associating supramolecular chemistry with corrosion are systematically discussed under two sections: (i) surface coatings and (ii) corrosion inhibitors that include supramolecular polymers, host-guest inclusion compounds, organic-inorganic hybrid materials, and supramolecular structures of graphene, crown ethers, self-assembled monolayers, etc. Different strategies for making antifouling surfaces based on block copolymers/gel systems, host-guest systems, and metal-organic structures are briefed. Cyclodextrin and mesoporous silica-based host-guest systems are extensively discussed, as they are the most prominent materials of current research interest. Future potentials for developments are presented. The review is expected to be beneficial to enhance supramolecular chemistry-related research and development in corrosion and biofouling prevention.

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9

Haino, Takeharu. "Supramolecular Chemistry: From Host-guest Complexes to Supramolecular Polymers." Journal of Synthetic Organic Chemistry, Japan 71, no. 11 (2013): 1172–81. http://dx.doi.org/10.5059/yukigoseikyokaishi.71.1172.

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10

Li, Zhan-Ting. "Supramolecular chemistry: from aromatic foldamers to solution-phase supramolecular organic frameworks." Beilstein Journal of Organic Chemistry 11 (November 2, 2015): 2057–71. http://dx.doi.org/10.3762/bjoc.11.222.

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This mini-review covers the growth, education, career, and research activities of the author. In particular, the developments of various folded, helical and extended secondary structures from aromatic backbones driven by different noncovalent forces (including hydrogen bonding, donor–acceptor, solvophobicity, and dimerization of conjugated radical cations) and solution-phase supramolecular organic frameworks driven by hydrophobically initiated aromatic stacking in the cavity of cucurbit[8]uril (CB[8]) are highlighted.

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11

Wu, Xialu, David J. Young, and T. S. Andy Hor. "A Molecular Artisans Guide to Supramolecular Coordination Complexes and Metal Organic Frameworks." Journal of Molecular and Engineering Materials 03, no. 01n02 (March 2015): 1540004. http://dx.doi.org/10.1142/s2251237315400043.

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As molecular synthesis advances, we are beginning to learn control of not only the chemical reactivity (and function) of molecules, but also of their interactions with other molecules. It is this basic idea that has led to the current explosion of supramolecular science and engineering. Parallel to this development, chemists have been actively pursuing the design of very large molecules using basic molecular building blocks. Herein, we review the general development of supramolecular chemistry and particularly of two new branches: supramolecular coordination complexes (SCCs) and metal organic frameworks (MOFs). These two fields are discussed in detail with typical examples to illustrate what is now possible and what challenges lie ahead for tomorrow's molecular artisans.

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12

Anslyn, Eric V. "Art, auto-mechanics, and supramolecular chemistry. A merging of hobbies and career." Beilstein Journal of Organic Chemistry 12 (February 26, 2016): 362–76. http://dx.doi.org/10.3762/bjoc.12.40.

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While the strict definition of supramolecular chemistry is “chemistry beyond the molecule”, meaning having a focus on non-covalent interactions, the field is primarily associated with the creation of synthetic receptors and self-assembly. For synthetic ease, the receptors and assemblies routinely possess a high degree of symmetry, which lends them an aspect of aesthetic beauty. Pictures of electron orbitals similarly can be seen as akin to works of art. This similarity was an early draw for me to the fields of supramolecular chemistry and molecular orbital theory, because I grew up in a household filled with art. In addition to art, my childhood was filled with repairing and constructing mechanical entities, such as internal combustion motors, where many components work together to achieve a function. Analogously, the field of supramolecular chemistry creates systems of high complexity that achieve functions or perform tasks. Therefore, in retrospect a career in supramolecular chemistry appears to be simply an extension of childhood hobbies involving art and auto-mechanics.

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13

Barooah, Nilotpal, and Jubaraj Baruah. "Supramolecular Chemistry with Phthalimide Derivatives." Mini-Reviews in Organic Chemistry 4, no. 4 (November 1, 2007): 292–309. http://dx.doi.org/10.2174/157019307782411680.

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14

Alahakoon, Sampath B., Shashini D. Diwakara, Christina M. Thompson, and Ronald A. Smaldone. "Supramolecular design in 2D covalent organic frameworks." Chemical Society Reviews 49, no. 5 (2020): 1344–56. http://dx.doi.org/10.1039/c9cs00884e.

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2D covalent organic frameworks (COFs) are a class of porous polymers with crystalline structures. This tutorial review discusses how the concepts of supramolecular chemistry are used to add form and function to COFs through their non-covalent bonds.

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15

Martín, Nazario, and Jean-François Nierengarten. "Supramolecular chemistry of fullerenes." Tetrahedron 62, no. 9 (February 2006): 1917. http://dx.doi.org/10.1016/j.tet.2005.12.050.

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16

Kroto, Harold W. "Supramolecular chemistry of fullerenes." Tetrahedron 62, no. 9 (February 2006): 1921. http://dx.doi.org/10.1016/j.tet.2005.12.051.

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17

Lehn, Jean-Marie. "Supramolecular chemistry of fullerenes." Tetrahedron 62, no. 9 (February 2006): 1919. http://dx.doi.org/10.1016/j.tet.2005.12.052.

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18

Lehn, Jean-Marie. "Supramolecular polymer chemistry." Macromolecular Symposia 174, no. 1 (September 2001): 5–6. http://dx.doi.org/10.1002/1521-3900(200109)174:1<5::aid-masy5>3.0.co;2-b.

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19

Tian, Jia, Lan Chen, Dan-Wei Zhang, Yi Liu, and Zhan-Ting Li. "Supramolecular organic frameworks: engineering periodicity in water through host–guest chemistry." Chemical Communications 52, no. 38 (2016): 6351–62. http://dx.doi.org/10.1039/c6cc02331b.

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20

Blanco-Gómez, Arturo, Pablo Cortón, Liliana Barravecchia, Iago Neira, Elena Pazos, Carlos Peinador, and Marcos D. García. "Controlled binding of organic guests by stimuli-responsive macrocycles." Chemical Society Reviews 49, no. 12 (2020): 3834–62. http://dx.doi.org/10.1039/d0cs00109k.

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21

Liu, Jiewei, Lianfen Chen, Hao Cui, Jianyong Zhang, Li Zhang, and Cheng-Yong Su. "Applications of metal–organic frameworks in heterogeneous supramolecular catalysis." Chem. Soc. Rev. 43, no. 16 (2014): 6011–61. http://dx.doi.org/10.1039/c4cs00094c.

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22

Li, Zhan-Ting. "ChemInform Abstract: Supramolecular Organic Chemistry. The Foldamer Approach." ChemInform 44, no. 25 (June 3, 2013): no. http://dx.doi.org/10.1002/chin.201325218.

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23

Descalzo, Ana B., Ramón Martínez-Máñez, Félix Sancenón, Katrin Hoffmann, and Knut Rurack. "The Supramolecular Chemistry of Organic–Inorganic Hybrid Materials." Angewandte Chemie International Edition 45, no. 36 (September 11, 2006): 5924–48. http://dx.doi.org/10.1002/anie.200600734.

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24

Lianglu, Juanzi, Weinan Hu, Xinju Zhu, Hong-Yu Zhang, Linlin Shi, Xin-Qi Hao, and Mao-Ping Song. "Synthesis of a Tetrahedral Metal–Organic Supramolecular Cage with Dendritic Carbazole Arms." International Journal of Molecular Sciences 23, no. 24 (December 8, 2022): 15580. http://dx.doi.org/10.3390/ijms232415580.

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In recent years, incredible endeavors have been devoted to the design and self-assembly of discrete metal–organic cages (MOCs) with expanding intricacy and functionality. The controlled synthesis of metal–organic supramolecular cages with large branched chains remains an interesting and challenging work in supramolecular chemistry. Herein, a tetrahedral metal–organic supramolecular cage (ZnII4L4) containing 12 dendritic carbazole arms is unprecedentedly constructed through coordination-driven subcomponent self-assembly and characterized in different ways. Interestingly, tetrahedral supramolecular Cage-1 exhibited the potential for aggregation-induced emission (AIE) performance and stimulus-responsive luminescence features, and it achieved color-tunable photoluminescence due to the introduction of dendritic carbazole arms. Crucially, owing to the great photophysical properties of Cage-1 in solution, Cage-1 was enabled to act as a fluorescent ink for the vapor-responsive recording and wiping of information.

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25

Cohen, Yoram, and Sarit Slovak. "Diffusion NMR for the characterization, in solution, of supramolecular systems based on calixarenes, resorcinarenes, and other macrocyclic arenes." Organic Chemistry Frontiers 6, no. 10 (2019): 1705–18. http://dx.doi.org/10.1039/c9qo00329k.

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The use of diffusion NMR in studying calixarenes and other arene-based supramolecular systems is described, emphasizing the pivotal role played by the calixarene community in transforming the methods into a routine tool used in supramolecular chemistry.

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26

Safarnejad Shad, Mastaneh, Pulikkal Veettil Santhini, and Wim Dehaen. "1,2,3-Triazolium macrocycles in supramolecular chemistry." Beilstein Journal of Organic Chemistry 15 (September 12, 2019): 2142–55. http://dx.doi.org/10.3762/bjoc.15.211.

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In this short review, we describe different pathways for synthesizing 1,2,3-triazolium macrocycles and focus on their application in different areas of supramolecular chemistry. The synthesis is mostly relying on the well-known “click reaction” (CuAAC) leading to 1,4-disubstituted 1,2,3-triazoles that then can be quaternized. Applications of triazolium macrocycles thus prepared include receptors for molecular recognition of anionic species, pH sensors, mechanically interlocked molecules, molecular machines, and molecular reactors.

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27

Bag, Braja Gopal, and Shaishab Kumar Dinda. "Arjunolic acid: A renewable template in supramolecular chemistry and nanoscience." Pure and Applied Chemistry 79, no. 11 (January 1, 2007): 2031–38. http://dx.doi.org/10.1351/pac200779112031.

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Arjunolic acid, a triterpenoid, renewably resourced from Terminalia arjuna sawdust, has the potential of being used as a structural molecular framework in supramolecular chemistry and nanoscience. The nanosized chiral triterpenoid on derivatization could immobilize varieties of organic solvents at low concentrations. The low-molecular-mass organic compounds self-assembled in organic media to form fibrous network structures having fibers of nano- to micrometer diameters. A dual-component supramolecular gelation has been demonstrated, exhibiting interesting thermochromic property. An arjunolic acid-derived crown ether showed efficient binding to monovalent cations, including a primary ammonium ion paving the way for chiral recognition of amino acids.

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28

Li, Zhan-Ting. "ChemInform Abstract: Supramolecular Chemistry: From Aromatic Foldamers to Solution-Phase Supramolecular Organic Frameworks." ChemInform 47, no. 12 (March 2016): no. http://dx.doi.org/10.1002/chin.201612242.

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29

Gao, Yuan, Yingying Dong, Qin Guo, Huanhuan Wang, Mei Feng, Zhengshen Yan, and Dong Bai. "Study on Supramolecules in Traditional Chinese Medicine Decoction." Molecules 27, no. 10 (May 19, 2022): 3268. http://dx.doi.org/10.3390/molecules27103268.

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With the application of the concept of supramolecular chemistry to various fields, a large number of supramolecules have been discovered. The chemical components of traditional Chinese medicine have various sources and unique structures. During the high-temperature boiling process, various active components form supramolecules due to complex interactions. The supramolecular structure in a traditional Chinese medicine decoction can not only be used as a drug carrier to promote the absorption and distribution of medicinal components but may also have biological activities superior to those of single active ingredients or their physical mixtures. By summarizing the relevant research results over recent years, this paper introduces the research progress regarding supramolecules in various decoctions, laying a foundation for further research into supramolecules in traditional Chinese medicine decoctions, and provides a new perspective for revealing the compatibility mechanisms of traditional Chinese medicine, guiding clinical medications, and developing new nanometers materials.

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30

Craig, Gavin A., Patrick Larpent, Hinano Urabe, Alexandre Legrand, Mickaele Bonneau, Shinpei Kusaka, and Shuhei Furukawa. "Hysteresis in the gas sorption isotherms of metal–organic cages accompanied by subtle changes in molecular packing." Chemical Communications 56, no. 25 (2020): 3689–92. http://dx.doi.org/10.1039/d0cc00932f.

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31

Waldvogel, Siegfried R. "A Practical Guide to Supramolecular Chemistry." Synthesis 2006, no. 9 (May 2006): 1556. http://dx.doi.org/10.1055/s-2006-941457.

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32

Pérez, Emilio M. "Energy, supramolecular chemistry, fullerenes, and the sky." Pure and Applied Chemistry 83, no. 1 (November 12, 2010): 201–11. http://dx.doi.org/10.1351/pac-con-10-09-22.

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The search for cleaner and more abundant sources of energy is one of the major scientific challenges of the 21st century. Owing to its privileged position as the central science, chemistry is bound to play a leading role in this quest. Within the search for new materials for organic photovoltaics, some of the work we have carried out concerning the supra-molecular chemistry of electron donor and acceptor molecules is presented.

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33

Olivo, Giorgio, Giorgio Capocasa, Daniele Del Giudice, Osvaldo Lanzalunga, and Stefano Di Stefano. "New horizons for catalysis disclosed by supramolecular chemistry." Chemical Society Reviews 50, no. 13 (2021): 7681–724. http://dx.doi.org/10.1039/d1cs00175b.

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Recent advancements in supramolecular catalysis are reviewed, which show the potential of related tools when applied to organic synthesis. Such tools are recognized as innovative instruments that can pave the way to alternative synthetic strategies.

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34

Zimmerman, Steven C. "A journey in bioinspired supramolecular chemistry: from molecular tweezers to small molecules that target myotonic dystrophy." Beilstein Journal of Organic Chemistry 12 (January 25, 2016): 125–38. http://dx.doi.org/10.3762/bjoc.12.14.

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This review summarizes part of the author’s research in the area of supramolecular chemistry, beginning with his early life influences and early career efforts in molecular recognition, especially molecular tweezers. Although designed to complex DNA, these hosts proved more applicable to the field of host–guest chemistry. This early experience and interest in intercalation ultimately led to the current efforts to develop small molecule therapeutic agents for myotonic dystrophy using a rational design approach that heavily relies on principles of supramolecular chemistry. How this work was influenced by that of others in the field and the evolution of each area of research is highlighted with selected examples.

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35

Stupp, Samuel I., and Liam C. Palmer. "Supramolecular Chemistry and Self-Assembly in Organic Materials Design." Chemistry of Materials 26, no. 1 (November 7, 2013): 507–18. http://dx.doi.org/10.1021/cm403028b.

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36

Gasparini, Giulio, Eun-Kyoung Bang, Javier Montenegro, and Stefan Matile. "ChemInform Abstract: Cellular Uptake: Lessons from Supramolecular Organic Chemistry." ChemInform 46, no. 33 (July 28, 2015): no. http://dx.doi.org/10.1002/chin.201533308.

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37

Han, Jin, and Chao Gao. "Host-Guest Supramolecular Chemistry of Dendritic Macromolecules." Current Organic Chemistry 15, no. 1 (January 1, 2011): 2–26. http://dx.doi.org/10.2174/138527211793797828.

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38

Kafarski, Pawel, Piotr Mlynarz, Ewa Rudzinska, and Lukasz Berlicki. "Organophosphorus Supramolecular Chemistry. Part 2. Organophosphorus Receptors." Current Organic Chemistry 11, no. 18 (December 1, 2007): 1593–609. http://dx.doi.org/10.2174/138527207783221192.

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39

Anderson, Tom W., G. Dan Pantoş, and Jeremy K. M. Sanders. "Supramolecular chemistry of monochiral naphthalenediimides." Organic & Biomolecular Chemistry 9, no. 21 (2011): 7547. http://dx.doi.org/10.1039/c1ob06147j.

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40

Barba‐Bon, Andrea, Mohamed Nilam, and Andreas Hennig. "Supramolecular Chemistry in the Biomembrane." ChemBioChem 21, no. 7 (April 2020): 886–910. http://dx.doi.org/10.1002/cbic.201900646.

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41

Howlader, Prodip, and Michael Schmittel. "Heteroleptic metallosupramolecular aggregates/complexation for supramolecular catalysis." Beilstein Journal of Organic Chemistry 18 (May 27, 2022): 597–630. http://dx.doi.org/10.3762/bjoc.18.62.

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Supramolecular catalysis is reviewed with an eye on heteroleptic aggregates/complexation. Since most of the current metallosupramolecular catalytic systems are homoleptic in nature, the idea of breaking/reducing symmetry has ignited a vivid search for heteroleptic aggregates that are made up by different components. Their higher degree of functional diversity and structural heterogeneity allows, as demonstrated by Nature by the multicomponent ATP synthase motor, a more detailed and refined configuration of purposeful machinery. Furthermore, (metallo)supramolecular catalysis is shown to extend beyond the single "supramolecular unit" and to reach far into the field and concepts of systems chemistry and information science.

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42

Turunen, Lotta, and Máté Erdélyi. "Halogen bonds of halonium ions." Chemical Society Reviews 49, no. 9 (2020): 2688–700. http://dx.doi.org/10.1039/d0cs00034e.

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43

Zaman, Md Badruz, Mohammad Rezaul Karim, Md Ashrafuzzaman, and Pejman Hanifi-Moghaddam. "Biomolecule conjugated nanoparticle synthons for detection of food contaminants." Canadian Journal of Chemistry 93, no. 9 (September 2015): 925–28. http://dx.doi.org/10.1139/cjc-2014-0588.

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This article investigates recent research on a series of photoluminescent nanoparticles (NPs) and supramolecular chemistry at their surface. This in turn prompts the concept of quantum dots supramolecular synthons (QDSS) and foresees the inevitable path towards biomimetics and bioinspired technology. We highlight the methodology how to create QDSS by functional assembly of photoluminescent semiconductors and the surface binding of supramolecular ligands.

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44

Yeung, Margaret Ching-Lam, and Vivian Wing-Wah Yam. "Luminescent cation sensors: from host–guest chemistry, supramolecular chemistry to reaction-based mechanisms." Chemical Society Reviews 44, no. 13 (2015): 4192–202. http://dx.doi.org/10.1039/c4cs00391h.

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This highlight provides a brief overview on luminescent cation detection strategies derived from a wide variety of organic and organometallic architectures, including those based on the ion-receptor complementarity, integrated with the extension of the concept of supramolecular chemistry and those using the irreversible analyte-specific reactions.

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45

Therrien, Bruno. "Thermotropic Liquid-Crystalline Materials Based on Supramolecular Coordination Complexes." Inorganics 8, no. 1 (December 22, 2019): 2. http://dx.doi.org/10.3390/inorganics8010002.

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Liquid crystals are among us, in living organisms and in electronic devices, and they have contributed to the development of our modern society. Traditionally developed by organic chemists, the field of liquid-crystalline materials is now involving chemists and physicists of all domains (computational, physical, inorganic, supramolecular, electro-chemistry, polymers, materials, etc.,). Such diversity in researchers confirms that the field remains highly active and that new applications can be foreseen in the future. In this review, liquid-crystalline materials developed around coordination complexes are presented, focusing on those showing thermotropic behavior, a relatively unexplored family of compounds.

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46

Bayer, Peter, Anja Matena, and Christine Beuck. "NMR Spectroscopy of supramolecular chemistry on protein surfaces." Beilstein Journal of Organic Chemistry 16 (October 9, 2020): 2505–22. http://dx.doi.org/10.3762/bjoc.16.203.

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As one of the few analytical methods that offer atomic resolution, NMR spectroscopy is a valuable tool to study the interaction of proteins with their interaction partners, both biomolecules and synthetic ligands. In recent years, the focus in chemistry has kept expanding from targeting small binding pockets in proteins to recognizing patches on protein surfaces, mostly via supramolecular chemistry, with the goal to modulate protein–protein interactions. Here we present NMR methods that have been applied to characterize these molecular interactions and discuss the challenges of this endeavor.

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47

Lv, Jing, Huibiao Liu, and Yuliang Li. "Self-assembly and properties of low-dimensional nanomaterials based on π-conjugated organic molecules." Pure and Applied Chemistry 80, no. 3 (January 1, 2008): 639–58. http://dx.doi.org/10.1351/pac200880030639.

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Building supramolecular architectures with well-defined shapes and functions is of great importance in materials science, nanochemistry, and biomimetic chemistry. In recent years, we have devoted much effort to the construction of well-defined supramolecular structures through noncovalent forces such as hydrogen bonding, π-stacking, metal-ligand bonds, and hydrophilic and hydrophobic interactions, with the aid of functional building blocks. The morphologies and their physical properties were studied, and new methods for the construction of one-dimensional nanoscale structures have been developed. In this review, we summarize our recent studies on the design and synthesis of the supramolecular systems, as well as the physical properties of nanoscale structures.

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48

Housecroft, Catherine E. "Coordination Polymers and Metal-Organic Frameworks: Structures and Applications—A Themed Issue in Honor of Professor Christoph Janiak on the Occasion of His 60th Birthday." Chemistry 3, no. 3 (July 28, 2021): 831–33. http://dx.doi.org/10.3390/chemistry3030060.

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This themed issue of Chemistry is in honor of Professor Christoph Janiak on the occasion of his 60th birthday, and celebrates his innovative contributions to the fields of supramolecular chemistry, coordination polymers, networks and metal-organic frameworks, inorganic/organic hybrid materials and inorganic materials from ionic liquids [...]

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49

Wong, Chun-Ho, and Steven C. Zimmerman. "Orthogonality in organic, polymer, and supramolecular chemistry: from Merrifield to click chemistry." Chemical Communications 49, no. 17 (2013): 1679. http://dx.doi.org/10.1039/c2cc37316e.

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50

Gerasko, O. A., M. N. Sokolov, and V. P. Fedin. "Mono- and polynuclear aqua complexes and cucurbit[6]uril: Versatile building blocks for supramolecular chemistry." Pure and Applied Chemistry 76, no. 9 (September 30, 2004): 1633–46. http://dx.doi.org/10.1351/pac200476091633.

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The review surveys new data on the directed construction of supramolecular organic–inorganic compounds from macrocyclic cavitand cucurbit[6]uril (C36H36N24O12)and mono- and polynuclear aqua complexes. Due to the presence of polarized carbonyl groups, cucurbit[6]uril forms strong complexes with alkali, alkaline earth and rare-earth metal ions, and hydrogen-bonded supramolecular adducts with cluster and polynuclear aqua complexes of transitional metals. A wide variety of supramolecular compounds and their unique structures are described.

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