We have designed and synthesized electron-rich calixarene derivatives, which undergo reversible electrochemical oxidation in a well-accessible potential range that allows the ready preparation and isolation of the corresponding cation radicals. Preparation of mono- or tetra-radical cation can be achieved by using stable aromatic cation-radical salts such as MA+•, MB+•, and NAP+• as selective organic oxidants. The cation radicals of calixarenes are stable indefinitely at ambient temperatures and can be readily characterized by UV-vis-NIR spectroscopy. These cation radicals bind a single molecule of nitric oxide within its cavity with remarkable efficiency
The direct observation of long-lived carbocations has represented a fascinating topic for chemists. ...
The condensation of ferrocene carbonylchloride (1) with p-t-butylcalix[4]arene (2) and calix[4]arene...
Le travail décrit dans ce mémoire constitue la première étude systématique entreprise jusqu'à ce jou...
We have designed and synthesized a modified calixarene derivative (1) that allows, for the first tim...
We have designed and synthesized a modified calixarene derivative that allows, for the first time, t...
The cyclic voltammetric properties of several substituted calix[4]arenes were examined in acetonitri...
Calixarenes are organic molecules which contain several aromatic units (in this work four) connected...
In the present thesis, both the published and the "ready-to-be-submitted" results concerning electro...
In this diploma thesis a detailed investigation of the step-by-step reduction mechanism of cone-mono...
The calix[4]arene skeleton is electrochemically inactive, but it is a useful stable frame for buil...
Calixarenes have found widespread application as building blocks for the design and synthesis of fun...
Calix[4]arene is a suitable inert and stable frame for building "smart" molecules and supramolecular...
The anodic oxidation of 25,27-dipropoxy-26-hydroxy-28-benzoyloxycalix[4]arene 1 and 25,27-dibenzyl-2...
Chemical modifications of calixarenes give rise to a great variety of derivatives with tuneable bind...
Calix[4]arene-based monoquinones having three efficient ligating groups of alkoxycarbomethyl ethers ...
The direct observation of long-lived carbocations has represented a fascinating topic for chemists. ...
The condensation of ferrocene carbonylchloride (1) with p-t-butylcalix[4]arene (2) and calix[4]arene...
Le travail décrit dans ce mémoire constitue la première étude systématique entreprise jusqu'à ce jou...
We have designed and synthesized a modified calixarene derivative (1) that allows, for the first tim...
We have designed and synthesized a modified calixarene derivative that allows, for the first time, t...
The cyclic voltammetric properties of several substituted calix[4]arenes were examined in acetonitri...
Calixarenes are organic molecules which contain several aromatic units (in this work four) connected...
In the present thesis, both the published and the "ready-to-be-submitted" results concerning electro...
In this diploma thesis a detailed investigation of the step-by-step reduction mechanism of cone-mono...
The calix[4]arene skeleton is electrochemically inactive, but it is a useful stable frame for buil...
Calixarenes have found widespread application as building blocks for the design and synthesis of fun...
Calix[4]arene is a suitable inert and stable frame for building "smart" molecules and supramolecular...
The anodic oxidation of 25,27-dipropoxy-26-hydroxy-28-benzoyloxycalix[4]arene 1 and 25,27-dibenzyl-2...
Chemical modifications of calixarenes give rise to a great variety of derivatives with tuneable bind...
Calix[4]arene-based monoquinones having three efficient ligating groups of alkoxycarbomethyl ethers ...
The direct observation of long-lived carbocations has represented a fascinating topic for chemists. ...
The condensation of ferrocene carbonylchloride (1) with p-t-butylcalix[4]arene (2) and calix[4]arene...
Le travail décrit dans ce mémoire constitue la première étude systématique entreprise jusqu'à ce jou...