2019
DOI: 10.1002/adma.201904824
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Supramolecular‐Macrocycle‐Based Crystalline Organic Materials

Abstract: macrocycles. They have been also employed to modify the surface properties of metal nanoparticles via noncovalent host−guest interactions, [31] covering their applications in drug delivery, [32] highly sensitive sensors, [33] selective catalysis, [34] and so on.In addition to their intensive applications based on their host−guest chemistry, macrocycles have also been used as building blocks to construct solid materials including porous organic polymers (POPs), [35,36] metal-organic frameworks (MOFs), [37][38][… Show more

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Cited by 133 publications
(120 citation statements)
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References 244 publications
(325 reference statements)
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“…It suggests that β-CD is capped on the end benzyl ring of ACAT (Figure 1b fully agreeing with the knowledge of cyclodextrin-based supramolecular chemistry in which the host-guest interaction is facilitated by hydrophobic effect and size matching. [33][34][35][36] In order to identify the stoichiometric ratio of ACAT-CD complex, the UV-Vis spectra of ACAT in the presence of β-CD with varied concentrations are summarized in Figure 1c. Accordingly, the absorbance at 530 nm which is ascribed to ACAT is dramatically increased upon the continuous addition of β-CD, accounting for the improved solubility of ACAT.…”
Section: Resultsmentioning
confidence: 99%
“…It suggests that β-CD is capped on the end benzyl ring of ACAT (Figure 1b fully agreeing with the knowledge of cyclodextrin-based supramolecular chemistry in which the host-guest interaction is facilitated by hydrophobic effect and size matching. [33][34][35][36] In order to identify the stoichiometric ratio of ACAT-CD complex, the UV-Vis spectra of ACAT in the presence of β-CD with varied concentrations are summarized in Figure 1c. Accordingly, the absorbance at 530 nm which is ascribed to ACAT is dramatically increased upon the continuous addition of β-CD, accounting for the improved solubility of ACAT.…”
Section: Resultsmentioning
confidence: 99%
“…first described that guest species could transport through the lattice of the crystals of p ‐tert‐butylcalix[4]arene along with the single crystal‐to‐single‐crystal transformations, although the fact that there is no obvious channels/porosity in its structure [1a] . During the past five years, NACs of pillararenes have attracted considerable interest as they display great potentials for practical applications, especially in the adsorption, separation, and storage of hydrocarbons [2–20] . In 2015, Ogoshi et al.…”
Section: Introductionmentioning
confidence: 99%
“…While the properties and applications of the robust pillararenes‐based NACs are well‐established, [2b,c, 18] new NACs based on pillararene derivatives and other important synthetic macrocycles, such as biphen[3]arene, [24] leaning pillar[6]arene (i.e., leaning tower[6]arene), [25] geminiarene, [26] bowtiearene, [27] cucurbit[6]uril, [23] hybrid[3]arene, [28] and tiara[5]arene [21] have been developed and recently reported. In this Minireview, we describe some important progress in the development of synthetic macrocycles‐based NACs, especially the constructions of NACs from newly discovered macrocyclic arenes for molecular separation and vapochromic application in the last two years.…”
Section: Introductionmentioning
confidence: 99%
“…The concepts of supramolecular chemistry provide a natural translation of molecule constructions to create functional materials. [1][2][3] Supramolecular assemblies containing extended p-conjugated macrocycles are particularly attractive for applications in organic electronics/devices, 4,5 examples of note include cyclic porphyrins, 6,7 annulenes, 8-10 phenylenes [11][12][13][14][15] and oligothiophenes. [16][17][18] The most common building blocks of p-extended macrocycles are phenylenes, ethynylenes, thiophenes and pyrroles.…”
Section: Introductionmentioning
confidence: 99%