2004
DOI: 10.1002/chem.200305496
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Shape‐Persistent Macrocycles: From Molecules to Materials

Abstract: Shape-persistent macrocycles with an interior in the nanometer regime allow the attachment of (functional) side groups at defined positions at the ring. These side groups can have either a fixed orientation relative to the molecular backbone or they can adapt their orientation according to an external stimulus. The properties and applications of the compounds depend strongly on the orientation of these side groups. Macrocycles with intraannular or adaptable long alkyl groups display a new design principle for … Show more

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Cited by 297 publications
(105 citation statements)
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References 76 publications
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“…Shape-persistent macrocycles with porous cavities, capable of forming ordered columnar structures, have been synthesized both by a geometry-driven and a templated approach. [51][52][53][54] However, few of these macrocycles possess an extended p-conjugation. [55,56] In order to check a new concept of extended conjugation length, para-coupled phenylene units were introduced instead of meta-coupled units.…”
Section: P-conjugated Polyphenylene Macrocyclesmentioning
confidence: 99%
“…Shape-persistent macrocycles with porous cavities, capable of forming ordered columnar structures, have been synthesized both by a geometry-driven and a templated approach. [51][52][53][54] However, few of these macrocycles possess an extended p-conjugation. [55,56] In order to check a new concept of extended conjugation length, para-coupled phenylene units were introduced instead of meta-coupled units.…”
Section: P-conjugated Polyphenylene Macrocyclesmentioning
confidence: 99%
“…[30,31,39,48] Appropriate peripheral decoration also enhances the self-assembly properties [33,34,49] of such shape-persistent macrocycles. [50][51][52] Continuing interest exists in probing the aromaticity [53] and antiaromaticity of these dehydroannulenes and other macrocyclic p-systems both experimentally and by advanced theoretical calculations. [54][55][56] A new synthetic methodology has been developed to prepare these carbon-rich compounds, adding to the main protocols, which remain oxidative acetylenic coupling to generate buta-1,3-diyne-1,4-diyl fragments [57] and Sonogashira crosscoupling [58,59] to form aryl-acetylenic bonds.…”
Section: Introductionmentioning
confidence: 99%
“…Self-assembled NC framelike arrays are of particular interest due to their unusual optical, electrical, and mechanical properties, as a consequence of the large surface-to-volume ratios that can be attained. These emerging materials offer promise in a broad range of applications including drug delivery and therapeutics (18,(21)(22)(23), novel materials for catalysis (24), optics (18,21), photonics (22,23), and as nanopatterned scaffolds (25,26).…”
mentioning
confidence: 99%