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Journal articles on the topic 'Supramolecular'

Author: Grafiati

Published: 4 June 2021

Last updated: 22 June 2024

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1

Peng, Kailin. "The applications of supramolecules in biological cells." Theoretical and Natural Science 4, no. 1 (April 28, 2023): 206–10. http://dx.doi.org/10.54254/2753-8818/4/20220550.

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A supramolecular structure is an ordered aggregate formed by intermolecular forces, also known as Van der Waals forces, and does not have to be covalent bonds. By combining with molecule with different structure, the supramolecule will show as a molecular collection with complex shape. It allows a supramolecule to have multiple characteristics and assume multiple functions. Without the need to synthesize by artificial initiative, supramolecules are widely apply in the biological field naturally. Many biological macromolecules are considered as one kind of supramolecules. These macromolecules can combine to form aggregations and, further, cell organelles, as well as collaborate to produce a series of biological reactions. Since supramolecules are a broad and cross majors research with rapid progress, it is necessary to regularly review, integrate and discuss this topic. Therefore, this review will discuss the present of supramolecules and analyze of application of supramolecules in cells. Recent research about how specific supramolecules apply and work for the particular function will be introduced.

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2

Zhang, Jie, Ling Qiu, Linshan Liu, Yang Liu, Peng Cui, Fang Wang, and Zhuxia Zhang. "Photoelectrochemical Response Enhancement for Metallofullerene-[12]Cycloparaphenylene Supramolecular Complexes." Nanomaterials 12, no. 9 (April 20, 2022): 1408. http://dx.doi.org/10.3390/nano12091408.

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The photoelectrochemical properties of three metallofullerene-[12]cycloparaphenylene ([12]CPP) supramolecular complexes of Sc3N@C78⊂[12]CPP, Sc3N@C80⊂[12]CPP, and Sc2C2@C82⊂[12]CPP were studied. It was revealed that the photocurrent responses of these supramolecular complexes show enhancement compared with those of pristine metallofullerenes, indicating the efficient photocurrent generation and promoted charge carrier transport caused by the supramolecular interaction. The results show that Sc2C2@C82 and Sc2C2@C82⊂[12]CPP have the strongest photocurrents. Then, by comparing the photocurrent intensities of the metallofullerene-biphenyl derivates mixture and the metallofullerene⊂[12]CPP complexes, it was demonstrated that the host–guest interaction is the key factor promoting photocurrent enhancement. At the same time, by observing the microscopic morphologies of pristine fullerenes and supramolecular complexes, it was found that the construction of supramolecules helps to improve the morphology of metallofullerenes on FTO glass. Additionally, their electrical conductivity in optoelectronic devices was tested, respectively, indicating that the construction of supramolecules facilitates the transport of charge carriers. This work discloses the potential application of metallofullerene supramolecular complexes as photodetector and photoelectronic materials.

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3

Yoshimoto, Soichiro, and Kingo Itaya. "Advances in supramolecularly assembled nanostructures of fullerenes and porphyrins at surfaces." Journal of Porphyrins and Phthalocyanines 11, no. 05 (May 2007): 313–33. http://dx.doi.org/10.1142/s1088424607000369.

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The ‘bottom-up’ strategy is an attractive and promising approach for the construction of nanoarchitectures. Supramolecular assemblies based on non-covalent interactions have been explored in an attempt to control surface properties. In this minireview, we focus on advances made in the past three years in the field of scanning tunneling microscopy (STM) on supramolecular assembly and the function of porphyrins, phthalocyanines, and fullerenes, non-covalently bound on metal single crystal surfaces. Well-defined adlayers, consisting of porphyrin and phthalocyanine for the design of supramolecular nanoarchitectures, supramolecular traps of C 60 on hydrogen bond networks, a unique approach for controlling molecular orientation by a 1:1 supramolecularly assembled film consisting of C 60 and the related derivatives and metallooctaethylporphyrins, and nanoapplications of fullerenes, either induced by tip manipulation or driven by thermal fluctuations at surfaces, were clearly visualized by STM.

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4

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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5

Zhang, Penghui, Yiran Liu, Xinkuo Fang, Li Ma, Yuanyuan Wang, and Lukang Ji. "Stoichiometric Ratio Controlled Dimension Transition and Supramolecular Chirality Enhancement in a Two-Component Assembly System." Gels 8, no. 5 (April 26, 2022): 269. http://dx.doi.org/10.3390/gels8050269.

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To control the dimension of the supramolecular system was of great significance. We construct a two component self-assembly system, in which the gelator LHC18 and achiral azobenzene carboxylic acid could co-assembly and form gels. By modulating the stoichiometric ratio of the two components, not only the morphology could be transformed from 1D nanaotube to 0D nanospheres but also the supramolecualr chirality could be tuned. This work could provide some insights to the control of dimension and the supramolecular chirality in the two-component systems by simply modulating the stoichiometric ratio.

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6

Zhang, Penghui, Yiran Liu, Xinkuo Fang, Li Ma, Yuanyuan Wang, and Lukang Ji. "Stoichiometric Ratio Controlled Dimension Transition and Supramolecular Chirality Enhancement in a Two-Component Assembly System." Gels 8, no. 5 (April 26, 2022): 269. http://dx.doi.org/10.3390/gels8050269.

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To control the dimension of the supramolecular system was of great significance. We construct a two component self-assembly system, in which the gelator LHC18 and achiral azobenzene carboxylic acid could co-assembly and form gels. By modulating the stoichiometric ratio of the two components, not only the morphology could be transformed from 1D nanaotube to 0D nanospheres but also the supramolecualr chirality could be tuned. This work could provide some insights to the control of dimension and the supramolecular chirality in the two-component systems by simply modulating the stoichiometric ratio.

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7

Chang, Hsiang-Yu, Yu-Ting Tseng, Zhiqin Yuan, Hung-Lung Chou, Ching-Hsiang Chen, Bing-Joe Hwang, Meng-Che Tsai, Huan-Tsung Chang, and Chih-Ching Huang. "The effect of ligand–ligand interactions on the formation of photoluminescent gold nanoclusters embedded in Au(i)–thiolate supramolecules." Physical Chemistry Chemical Physics 19, no. 19 (2017): 12085–93. http://dx.doi.org/10.1039/c7cp01915g.

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8

Liu, Bing, Tao Yang, Xin Mu, Zhijian Mai, Hao Li, Yao Wang, and Guofu Zhou. "Smart Supramolecular Self-Assembled Nanosystem: Stimulus-Responsive Hydrogen-Bonded Liquid Crystals." Nanomaterials 11, no. 2 (February 10, 2021): 448. http://dx.doi.org/10.3390/nano11020448.

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In a liquid crystal (LC) state, specific orientations and alignments of LC molecules produce outstanding anisotropy in structure and properties, followed by diverse optoelectronic functions. Besides organic LC molecules, other nonclassical components, including inorganic nanomaterials, are capable of self-assembling into oriented supramolecular LC mesophases by non-covalent interactions. Particularly, huge differences in size, shape, structure and properties within these components gives LC supramolecules higher anisotropy and feasibility. Therefore, hydrogen bonds have been viewed as the best and the most common option for supramolecular LCs, owing to their high selectivity and directionality. In this review, we summarize the newest advances in self-assembled structure, stimulus-responsive capability and application of supramolecular hydrogen-bonded LC nanosystems, to provide novel and immense potential for advancing LC technology.

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9

Li, Jun. "Supramolecular Polymers for Potential Biomedical Applications." Advanced Materials Research 410 (November 2011): 94–97. http://dx.doi.org/10.4028/www.scientific.net/amr.410.94.

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The phenomena of molecular self-assembly have inspired interesting development of novel functional materials. We have been focusing on developing novel polymers with the ability to self-assemble into novel supramolecular structures, which can function as biomaterials for potential drug/gene delivery and tissue engineering applications. The key components in our macromolecular self-assembling structures include the biodegradable and biocompatible microbial biopolyesters, poly (β-hydroxyalkanoates), and the macrocyclic polysaccharides, cyclodextrins. A series of novel block copolymers and interlocked supramolecular architectures were designed and synthesized. They were characterized in terms of their molecular and supramolecular structures, as well as their properties and functions as biomaterials for potential drug and gene delivery, and tissue engineering applications. Amphiphilic block copolymers of different chain architectures composed of poly [(R)-3-hydroxybutyrate] as hydrophobic segments, and poly (ethylene glycol), poly (propylene glycol), or poly (N-isopropylacrylamide) as hydrophilic segments were synthesized. They could self-assemble to form stable micelles, nanopatterning thin films, and thermo-sensitive hydrogels, which were demonstrated to be promising potential biomaterials for controlled and sustained delivery of drugs and tissue engineering scaffolding materials. The self-assembly of block copolymers with cyclodextrins resulted in supramolecular hydrogels and cationic supramolecules, which were used as injectable drug delivery systems, and novel polymeric gene delivery vectors.

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10

Bai, Peter, Joseph Kao, Jian-Hao Chen, William Mickelson, Alex Zettl, and Ting Xu. "Nanostructures on graphene using supramolecule and supramolecular nanocomposites." Nanoscale 6, no. 9 (2014): 4503–7. http://dx.doi.org/10.1039/c4nr00420e.

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11

Vicens, Jacques, and Quentin Vicens. "Emergences of supramolecular chemistry: from supramolecular chemistry to supramolecular science." Journal of Inclusion Phenomena and Macrocyclic Chemistry 71, no. 3-4 (June 30, 2011): 251–74. http://dx.doi.org/10.1007/s10847-011-0001-z.

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12

ARAKI, Koji, Jun LI, and Isao YOSHIKAWA. "From Supramolecular Polymers to Supramolecular Materials." Oleoscience 5, no. 6 (2005): 265–72. http://dx.doi.org/10.5650/oleoscience.5.265.

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13

WANG, Xiu-Feng, Li ZHANG, and Ming-Hua LIU. "supramolecular Gels: Structural Diversity and supramolecular Chirality." Acta Physico-Chimica Sinica 32, no. 1 (2016): 227–38. http://dx.doi.org/10.3866/pku.whxb201511181.

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14

Goshe, Andrew J., and B. Bosnich. "Supramolecular Chemistry. Supramolecular Rectangles and Their Guests." Synlett 2001, Special Issue (2001): 0941–44. http://dx.doi.org/10.1055/s-2001-14628.

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15

Fox, Justin D., and Stuart J. Rowan. "Supramolecular Polymerizations and Main-Chain Supramolecular Polymers." Macromolecules 42, no. 18 (September 22, 2009): 6823–35. http://dx.doi.org/10.1021/ma901144t.

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16

Wu, Shuanggen, Changyong Cai, Fenfang Li, Zhijian Tan, and Shengyi Dong. "Deep Eutectic Supramolecular Polymers: Bulk Supramolecular Materials." Angewandte Chemie 132, no. 29 (May 11, 2020): 11969–73. http://dx.doi.org/10.1002/ange.202004104.

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17

Wu, Shuanggen, Changyong Cai, Fenfang Li, Zhijian Tan, and Shengyi Dong. "Deep Eutectic Supramolecular Polymers: Bulk Supramolecular Materials." Angewandte Chemie International Edition 59, no. 29 (May 11, 2020): 11871–75. http://dx.doi.org/10.1002/anie.202004104.

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18

Li, Yilin, Yuteng Su, Zhaoxiang Li, and Yueyue Chen. "Supramolecular Combination Cancer Therapy Based on Macrocyclic Supramolecular Materials." Polymers 14, no. 22 (November 11, 2022): 4855. http://dx.doi.org/10.3390/polym14224855.

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Supramolecular combination therapy adopts supramolecular materials to design intelligent drug delivery systems with different strategies for cancer treatments. Thereinto, macrocyclic supramolecular materials play a crucial role in encapsulating anticancer drugs to improve anticancer efficiency and decrease toxicity towards normal tissue by host–guest interaction. In general, chemotherapy is still common therapy for solid tumors in clinics. However, supramolecular combination therapy can overcome the limitations of the traditional single-drug chemotherapy in the laboratory findings. In this review, we summarized the combination chemotherapy, photothermal chemotherapy, and gene chemotherapy based on macrocyclic supramolecular materials. Finally, the application prospects in supramolecular combination therapy are discussed.

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19

D'Souza, Francis, Suresh Gadde, Mohamed E. El-Khouly, Melvin E. Zandler, Yasuyaki Araki, and Osamu Ito. "A supramolecular Star Wars Tie Fighter Ship: electron transfer in a self-assembled triad composed of two zinc naphthalocyanines and a fullerene." Journal of Porphyrins and Phthalocyanines 09, no. 10 (October 2005): 698–705. http://dx.doi.org/10.1142/s1088424605000812.

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Photoactive supramolecules composed of electron donor and electron acceptor entities are important for light energy harvesting applications. In the present study, a Star Wars Tie Fighter Ship shaped supramolecular triad was constructed by self-assembling two zinc naphthalocyanines to a fulleropyrrolidine bearing two pyridine entities using an axial coordination approach. Optical absorption and emission studies revealed stable complex formation, and the experimentally determined free-energy change revealed the possibility of electron transfer from singlet excited zinc naphthalocyanine to the fulleropyrrolidine. The picosecond time-resolved emission technique was utilized to evaluate the kinetics of charge separation while nanosecond transient absorption spectral studies provided evidence for electron transfer quenching. The measured charge-separation rate, k CS and quantum yield, Φ CS were found to be 5.7 × 109 s −1 and 0.93 in toluene, respectively, indicating an efficient process within the supramolecular triad. The charge recombination rate (k CR ) of the supramolecular ion-pair calculated from the nanosecond transient absorption technique was found to be 3.5 × 107 s −1 yielding a lifetime for the radical ion-pair (τ RIP ) of about 30 ns. Changing the solvent from the noncoordinating toluene to the coordinating benzonitrile or THF destroyed the supramolecular structure, and under these experimental conditions, only intermolecular electron transfer from the triplet excited zinc naphthalocyanine to fulleropyrrolidine could be observed. Under these conditions, the measured electron transfer rates, k et , T inter , were found to be 2.6 × 107 M −1. s −1 in benzonitrile and 1.2 × 107 M −1. s −1 in THF, respectively.

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20

Cui, Honggang, and Bing Xu. "Supramolecular medicine." Chem. Soc. Rev. 46, no. 21 (2017): 6430–32. http://dx.doi.org/10.1039/c7cs90102j.

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Guest editors Honggang Cui and Bing Xu introduce the supramolecular medicine issue of Chemical Society Reviews. In a broader context, Supramolecular Medicine can be defined as the supramolecular formulation of diagnostic and therapeutic agents for the diagnosis, treatment, and prevention of disease.

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21

Barata, Patrícia D., Alexandra I. Costa, Sérgio Costa, and José V. Prata. "Fluorescent Bis-Calix[4]arene-Carbazole Conjugates: Synthesis and Inclusion Complexation Studies with Fullerenes C60 and C70." Molecules 26, no. 16 (August 18, 2021): 5000. http://dx.doi.org/10.3390/molecules26165000.

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Supramolecular chemistry has become a central theme in chemical and biological sciences over the last decades. Supramolecular structures are being increasingly used in biomedical applications, particularly in devices requiring specific stimuli-responsiveness. Fullerenes, and supramolecular assemblies thereof, have gained great visibility in biomedical sciences and engineering. Sensitive and selective methods are required for the study of their inclusion in complexes in various application fields. With this in mind, two new fluorescent bis-calix[4]arene-carbazole conjugates (4 and 5) have been designed. Herein, their synthesis and ability to behave as specific hosts for fullerenes C60 and C70 is described. The optical properties of the novel compounds and their complexes with C60 and C70 were thoroughly studied by UV-Vis and steady-state and time-resolved fluorescence spectroscopies. The association constants (Ka) for the complexation of C60 and C70 by 4 and 5 were determined by fluorescence techniques. A higher stability was found for the C70@4 supramolecule (Ka = 5.6 × 104 M−1; ΔG = −6.48 kcal/mol). Evidence for the formation of true inclusion complexes between the host 4 and C60/C70 was obtained from NMR spectroscopy performed at low temperatures. The experimental findings were fully corroborated by density functional theory (DFT) models performed on the host–guest assemblies (C60@4 and C70@4).

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22

Yamamoto, Hiroshi M., Ryoko Maeda, Jun-ichi Yamaura, and Reizo Kato. "Multicomponent molecular conductors with supramolecular assembly — supramolecules with various dimensionality—." Synthetic Metals 120, no. 1-3 (March 2001): 781–82. http://dx.doi.org/10.1016/s0379-6779(00)00881-x.

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23

Cheng, Xiaoxiao, Tengfei Miao, Yilin Qian, Zhengbiao Zhang, Wei Zhang, and Xiulin Zhu. "Supramolecular Chirality in Azobenzene-Containing Polymer System: Traditional Postpolymerization Self-Assembly Versus In Situ Supramolecular Self-Assembly Strategy." International Journal of Molecular Sciences 21, no. 17 (August 27, 2020): 6186. http://dx.doi.org/10.3390/ijms21176186.

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Recently, the design of novel supramolecular chiral materials has received a great deal of attention due to rapid developments in the fields of supramolecular chemistry and molecular self-assembly. Supramolecular chirality has been widely introduced to polymers containing photoresponsive azobenzene groups. On the one hand, supramolecular chiral structures of azobenzene-containing polymers (Azo-polymers) can be produced by nonsymmetric arrangement of Azo units through noncovalent interactions. On the other hand, the reversibility of the photoisomerization also allows for the control of the supramolecular organization of the Azo moieties within polymer structures. The construction of supramolecular chirality in Azo-polymeric self-assembled system is highly important for further developments in this field from both academic and practical points of view. The postpolymerization self-assembly strategy is one of the traditional strategies for mainly constructing supramolecular chirality in Azo-polymers. The in situ supramolecular self-assembly mediated by polymerization-induced self-assembly (PISA) is a facile one-pot approach for the construction of well-defined supramolecular chirality during polymerization process. In this review, we focus on a discussion of supramolecular chirality of Azo-polymer systems constructed by traditional postpolymerization self-assembly and PISA-mediated in situ supramolecular self-assembly. Furthermore, we will also summarize the basic concepts, seminal studies, recent trends, and perspectives in the constructions and applications of supramolecular chirality based on Azo-polymers with the hope to advance the development of supramolecular chirality in chemistry.

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24

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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25

Wang, Wei, Yu-Xuan Wang, and Hai-Bo Yang. "Supramolecular transformations within discrete coordination-driven supramolecular architectures." Chemical Society Reviews 45, no. 9 (2016): 2656–93. http://dx.doi.org/10.1039/c5cs00301f.

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In this review, a comprehensive summary of supramolecular transformations within discrete coordination-driven supramolecular architectures, including helices, metallacycles, metallacages, etc., is presented.

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26

Moore, Jeffrey S. "Supramolecular Materials." MRS Bulletin 25, no. 4 (April 2000): 26–29. http://dx.doi.org/10.1557/mrs2000.25.

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This issue of MRS Bulletin is devoted to the subject of supramolecular materials. The term supramolecular is widely used to describe the intentional use of noncovalent interactions to bring about a desired arrangement of molecules. As the articles in this issue illustrate, this type of molecular engineering can provide structural control on the nanoscale and beyond, broadly impacting the properties of the resulting materials. The goal is to create a collection of molecules in which the whole possesses characteristics that are different and unattainable from the individual components.

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27

Brunsveld, Luc, Brigitte J. B. Folmer, and E. W. Meijer. "Supramolecular Polymers." MRS Bulletin 25, no. 4 (April 2000): 49–53. http://dx.doi.org/10.1557/mrs2000.29.

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What started as a scientific challenge roughly 10 years ago has become a technological reality today, as materials from supramolecular polymers and their many applications as smart materials have emerged. Synthetic polymeric materials are among the most important classes of new materials introduced in the 20th century. They are primarily used for construction, but electronic and biomedical applications are also at the forefront of science and technology.

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28

Chen, Xiaoyuan, Gang Zheng, Jianjun Cheng, and Yi-Yan Yang. "Supramolecular Nanotheranostics." Theranostics 9, no. 11 (2019): 3014–16. http://dx.doi.org/10.7150/thno.36788.

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29

Lehn, Jean-Marie. "Supramolecular chemistry." Proceedings / Indian Academy of Sciences 106, no. 5 (October 1994): 915–22. http://dx.doi.org/10.1007/bf02841907.

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30

Webber, Matthew J., Eric A. Appel, E. W. Meijer, and Robert Langer. "Supramolecular biomaterials." Nature Materials 15, no. 1 (December 18, 2015): 13–26. http://dx.doi.org/10.1038/nmat4474.

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31

Amabilino, David B., David K. Smith, and Jonathan W. Steed. "Supramolecular materials." Chemical Society Reviews 46, no. 9 (2017): 2404–20. http://dx.doi.org/10.1039/c7cs00163k.

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32

Rosing, J., and H. C. Hemker. "Supramolecular Biology." Pathophysiology of Haemostasis and Thrombosis 32, no. 1 (2002): 1. http://dx.doi.org/10.1159/000057281.

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33

Wilson, Andrew J. "Supramolecular chemistry." Annual Reports Section "B" (Organic Chemistry) 102 (2006): 148. http://dx.doi.org/10.1039/b515110b.

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34

Gerhardt, Warren W., Anthony J. Zucchero, James N. Wilson, Clinton R. South, Uwe H. F. Bunz, and Marcus Weck. "Supramolecular cruciforms." Chemical Communications, no. 20 (2006): 2141. http://dx.doi.org/10.1039/b602087a.

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35

de Greef, Tom F. A., and E. W. Meijer. "Supramolecular polymers." Nature 453, no. 7192 (May 2008): 171–73. http://dx.doi.org/10.1038/453171a.

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36

Yang, Cheng, and Yoshihisa Inoue. "Supramolecular photochirogenesis." Chem. Soc. Rev. 43, no. 12 (2014): 4123–43. http://dx.doi.org/10.1039/c3cs60339c.

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37

Bohne, Cornelia. "Supramolecular dynamics." Chem. Soc. Rev. 43, no. 12 (2014): 4037–50. http://dx.doi.org/10.1039/c3cs60352k.

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38

Jorgensen, W. L. "Supramolecular chemistry." Proceedings of the National Academy of Sciences 90, no. 5 (March 1, 1993): 1635–36. http://dx.doi.org/10.1073/pnas.90.5.1635.

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39

Huang, Feihe, and Oren A. Scherman. "Supramolecular polymers." Chemical Society Reviews 41, no. 18 (2012): 5879. http://dx.doi.org/10.1039/c2cs90071h.

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40

McCoy, Colin P. "Supramolecular Chemistry." Synthesis 2002, no. 03 (2002): 438. http://dx.doi.org/10.1055/s-2002-20023.

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41

Lehn, J. "Supramolecular chemistry." Science 260, no. 5115 (June 18, 1993): 1762–63. http://dx.doi.org/10.1126/science.8511582.

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42

Dalgarno, Scott J. "Supramolecular chemistry." Annual Reports Section "B" (Organic Chemistry) 105 (2009): 190. http://dx.doi.org/10.1039/b822055g.

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43

Rodríguez-Llansola, Francisco, and E. W. Meijer. "Supramolecular Autoregulation." Journal of the American Chemical Society 135, no. 17 (April 17, 2013): 6549–53. http://dx.doi.org/10.1021/ja4006833.

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44

Tian, Jian. "Supramolecular chemistry." Annual Reports Section "B" (Organic Chemistry) 108 (2012): 171. http://dx.doi.org/10.1039/c2oc90020c.

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45

Nardin, Corinne, and Joachim Kohn. "Supramolecular Polymers." Materials Research Bulletin 37, no. 7 (June 2002): 1377–79. http://dx.doi.org/10.1016/s0025-5408(02)00755-9.

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46

DAGANI, RON. "SUPRAMOLECULAR POLYMERS." Chemical & Engineering News 75, no. 48 (December 1997): 4. http://dx.doi.org/10.1021/cen-v075n048.p004.

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47

Takata, Toshikazu. "Supramolecular polymers." Polymer 128 (October 2017): 242. http://dx.doi.org/10.1016/j.polymer.2017.09.030.

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48

Cacialli, Franco, Paolo Samorì, and Carlos Silva. "Supramolecular architectures." Materials Today 7, no. 4 (April 2004): 24–32. http://dx.doi.org/10.1016/s1369-7021(04)00186-5.

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49

Karabıyık, Hande, Resul Sevinçek, and Hasan Karabıyık. "Supramolecular aromaticity." Journal of Molecular Structure 1064 (May 2014): 135–49. http://dx.doi.org/10.1016/j.molstruc.2014.02.010.

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Gibb, Bruce C. "Supramolecular Stereochemistry." Journal of Supramolecular Chemistry 2, no. 1-3 (January 2002): 123–31. http://dx.doi.org/10.1016/s1472-7862(02)00088-6.

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