6533b81ffe1ef96bd1278fb2

RESEARCH PRODUCT

Trapping and Reactivity of a Molecular Aluminium Oxide Ion

Petra VaskoPetra VaskoSimon AldridgeJamie HicksJose M. GoicoecheaAndreas Heilmann

subject

small molecule activationOxidereduction010402 general chemistry01 natural sciencesHeterolysisCatalysischemistry.chemical_compoundPolymer chemistryMoleculeReactivity (chemistry)alumiiniBond cleavageAluminium oxides010405 organic chemistryaluminiumpelkistysGeneral MedicineGeneral Chemistrykompleksiyhdisteet0104 chemical sciencesHyponitritechemistryoksiditAluminium oxidealuminyloxide

description

Aluminium oxides constitute an important class of inorganic compound that are widely exploited in the chemical industry as catalysts and catalyst supports. Due to the tendency for such systems to aggregate via Al‐O‐Al bridges, the synthesis of well‐defined, soluble, molecular models for these materials is challenging. Here we show that reactions of the potassium aluminyl complex K 2 [( NON )Al] 2 ( NON = 4,5‐bis(2,6‐diiso‐propylanilido)‐2,7‐di‐tert‐butyl‐9,9‐dimethylxanthene) with CO 2 , PhNCO and N 2 O all proceed via a common aluminium oxide intermediate. This highly reactive species can be trapped by coordination of a THF molecule as the anionic oxide complex [( NON )AlO(THF)] ‐ , which features discrete Al‐O bonds and dimerizes in the solid state via weak O … K interactions. This species reacts with a range of small molecules including N 2 O to give a hyponitrite ([N 2 O 2 ] 2‐ ) complex and H 2 , the latter offering an unequivocal example of heterolytic E‐H bond cleavage across a main group M‐O bond. peerReviewed

http://urn.fi/URN:NBN:fi:jyu-201910114407