Macrocyclic molecules containing appropriate binding sites and cavities of suitable size and shape may be designed to form selective inclusion complexes. Actu- ally, the molecular topology of the host molecule can be synthetically modulated in order to bind many different chemical species. For this purpose, aza macrocyclic receptors able to bind different kinds of substrates, such as inorganic or organic cation or anionic specie have been studied to elaborate their use as selective host molecules, molecular carriers, and catalysts. We have therefore devised a synthetic procedure able to produce, in high yield, very large azamacrocycles

Synthetic route to produce Giant-Siaze azamacrocycles / C.Bazzicalupi; A.Bencini; V.Fusi; M.Micheloni; P.Paoletti; B.Valtancoli. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - STAMPA. - 59:(1994), pp. 7508-7510.

Synthetic route to produce Giant-Siaze azamacrocycles

BAZZICALUPI, CARLA;BENCINI, ANDREA;VALTANCOLI, BARBARA
1994

Abstract

Macrocyclic molecules containing appropriate binding sites and cavities of suitable size and shape may be designed to form selective inclusion complexes. Actu- ally, the molecular topology of the host molecule can be synthetically modulated in order to bind many different chemical species. For this purpose, aza macrocyclic receptors able to bind different kinds of substrates, such as inorganic or organic cation or anionic specie have been studied to elaborate their use as selective host molecules, molecular carriers, and catalysts. We have therefore devised a synthetic procedure able to produce, in high yield, very large azamacrocycles
1994
59
7508
7510
C.Bazzicalupi; A.Bencini; V.Fusi; M.Micheloni; P.Paoletti; B.Valtancoli
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/326782
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