A novel approach to cucurbituril synthesis is described where partial substitution is introduced into cucurbit[n]uril. The identification of homologues (and their substitution) in reaction mixtures is achieved by a combination of ESMS and the use of the molecular probes (guests) 1,4-dioxane and 1,9-octanediamine. A unique symmetrical hexamethylcucurbit[3,3]uril, the major product, was isolated and characterized
Cucurbiturils (CB[n]) are macrocyclic compounds made from glycoluril monomers. They have the potenti...
Cucurbit[n]uril (CB[n]) is a unique macrocycle that can bind small molecules with promising potentia...
Cucurbiturils (CB[n]) are macrocyclic compounds made from glycoluril monomers. They have the potenti...
A novel approach to cucurbituril synthesis is described where partial substitution is introduced int...
Classical cucurbit[n]uril (Q[n], n = 5 to 10) are macrocyclic structures resembling a hollow pumpkin...
The supramolecular chemistry of cucurbituril, a synthetic receptor, is fascinating because of the re...
The recently discovered cucurbit[n]uril are a range of macrocyclic hosts which have enormous potenti...
This dissertation investigates the inclusion complexation behavior of various guest molecules with h...
The characterization of a mixture of cucurbit[n]uril (n = 6,7,8) was carried out by MALDI MS (Matrix...
The cucurbit[n]uril (Q[n]) family provides real potential for a wide range of applications, includin...
Cucurbit[n]uril, CB[n], is made from the condensation of glycoluril and formaldehyde in concentrated...
International audienceWe describe a photochemical method to introduce a single alcohol function dire...
We describe a photochemical method to introduce a single alcohol function directly on cucurbit[n]uri...
International audienceWe describe a photochemical method to introduce a single alcohol function dire...
International audienceWe describe a photochemical method to introduce a single alcohol function dire...
Cucurbiturils (CB[n]) are macrocyclic compounds made from glycoluril monomers. They have the potenti...
Cucurbit[n]uril (CB[n]) is a unique macrocycle that can bind small molecules with promising potentia...
Cucurbiturils (CB[n]) are macrocyclic compounds made from glycoluril monomers. They have the potenti...
A novel approach to cucurbituril synthesis is described where partial substitution is introduced int...
Classical cucurbit[n]uril (Q[n], n = 5 to 10) are macrocyclic structures resembling a hollow pumpkin...
The supramolecular chemistry of cucurbituril, a synthetic receptor, is fascinating because of the re...
The recently discovered cucurbit[n]uril are a range of macrocyclic hosts which have enormous potenti...
This dissertation investigates the inclusion complexation behavior of various guest molecules with h...
The characterization of a mixture of cucurbit[n]uril (n = 6,7,8) was carried out by MALDI MS (Matrix...
The cucurbit[n]uril (Q[n]) family provides real potential for a wide range of applications, includin...
Cucurbit[n]uril, CB[n], is made from the condensation of glycoluril and formaldehyde in concentrated...
International audienceWe describe a photochemical method to introduce a single alcohol function dire...
We describe a photochemical method to introduce a single alcohol function directly on cucurbit[n]uri...
International audienceWe describe a photochemical method to introduce a single alcohol function dire...
International audienceWe describe a photochemical method to introduce a single alcohol function dire...
Cucurbiturils (CB[n]) are macrocyclic compounds made from glycoluril monomers. They have the potenti...
Cucurbit[n]uril (CB[n]) is a unique macrocycle that can bind small molecules with promising potentia...
Cucurbiturils (CB[n]) are macrocyclic compounds made from glycoluril monomers. They have the potenti...