La re´activite´ des groupes amino des quelques dialkyle esters de l' acide 2,6-diamino-benzo[1,2-b:4,5-b0]difuran-3,7-dicarboxylique vers des re´actants acyliques a e´te´ enque^te´. L'accomplissement facile et chemose´lectif des de´rivatives N,N0-acetyl- et N,N0-benzoyl- rend les compose´s des monome`res approprie´s a` obtenir des polyme`res avec un comportement chemo-physique modulable. Deux nouvelles polyamides, potentiellement utiles pour des applications dans le domaine de l'e´lectronique organique, ont e´te´ synthe´tise´s et on a examine´ leur proprie´te´s. Une analyse comple`te aux rayons X a e´te´ re´alise´e sur quelques-uns des compose´s pour obtenir des informations sur l'extension de la conjugaison e´lectronique. L'accomplissement du de´riva^t oxazinone avec une re´action de cyclisation de l'ester N-N0-benzoyl est aussi de´crite.

The reactivity of amino groups of some dialkyl esters of 2,6-diamino-benzo[1,2-b:4,5-b0]difuran-3,7-dicarboxylic acid towards acylic reactants was investigated. The easy and chemoselective obtainment of the N,N0-acetyl- and N,N0-benzoyl-derivatives makes the diamino compounds suitable monomers to prepare polymers with tunable chemo-physical behavior. Two novel polyamides, potentially useful for applications in the field of organic electronics, were synthesized and their properties examined. Single crystal X-ray analysis was performed on some of the prepared compounds, thus obtaining information on the extent of electronic conjugation. The obtainment of an oxazinone derivative by cyclization reaction of an N,N0-benzoyl ester was also described

Synthesis, structure and reactivity of amino-benzodifurane derivatives

2009

Abstract

The reactivity of amino groups of some dialkyl esters of 2,6-diamino-benzo[1,2-b:4,5-b0]difuran-3,7-dicarboxylic acid towards acylic reactants was investigated. The easy and chemoselective obtainment of the N,N0-acetyl- and N,N0-benzoyl-derivatives makes the diamino compounds suitable monomers to prepare polymers with tunable chemo-physical behavior. Two novel polyamides, potentially useful for applications in the field of organic electronics, were synthesized and their properties examined. Single crystal X-ray analysis was performed on some of the prepared compounds, thus obtaining information on the extent of electronic conjugation. The obtainment of an oxazinone derivative by cyclization reaction of an N,N0-benzoyl ester was also described
2009
Istituto di Biostrutture e Bioimmagini - IBB - Sede Napoli
La re´activite´ des groupes amino des quelques dialkyle esters de l' acide 2,6-diamino-benzo[1,2-b:4,5-b0]difuran-3,7-dicarboxylique vers des re´actants acyliques a e´te´ enque^te´. L'accomplissement facile et chemose´lectif des de´rivatives N,N0-acetyl- et N,N0-benzoyl- rend les compose´s des monome`res approprie´s a` obtenir des polyme`res avec un comportement chemo-physique modulable. Deux nouvelles polyamides, potentiellement utiles pour des applications dans le domaine de l'e´lectronique organique, ont e´te´ synthe´tise´s et on a examine´ leur proprie´te´s. Une analyse comple`te aux rayons X a e´te´ re´alise´e sur quelques-uns des compose´s pour obtenir des informations sur l'extension de la conjugaison e´lectronique. L'accomplissement du de´riva^t oxazinone avec une re´action de cyclisation de l'ester N-N0-benzoyl est aussi de´crite.
Polycycles
Amino-benzodifurane
Polymers
X-ray diffraction structures
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/123111
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