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Your search keyword '"Majzik, Z."' showing total 2 results
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2 results on '"Majzik, Z."'

1. Synthesis of a naphthodiazaborole and its verification by planarization with AFM

Author

Fernández, E., Majzik, Z, Cuenca, A. B., Pavlicek, N., Miralles, N., Meyer, G., Gross, L., Organometàl.lics i Catàlisi Homogènia, Química Física i Inorgànica, and Universitat Rovira i Virgili

Subjects
Chemistry, Funcional de densitat, Teoria del, STM, Bdan, 1936-0851, Química, AFM
Abstract

Aiming to develop materials with new functionalities, we designed the synthesis of a naphthodiazaborinine (the BN isoster of the phenalenyl anion) that is bonded to a hindered di-orthosubstituted aryl system (9-anthracene). We used atomic force microscopy (AFM) to verify the structure of the molecule synthesized. To determine it unambiguously, we planarized the originally nonplanar molecule by removing H atoms that cause steric hindrance.

Published
2016
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2. Synthesis of a naphthodiazaborole and its verification by planarization with AFM

Author

Fernández, E., Majzik, Z, Cuenca, A. B., Pavlicek, N., Miralles, N., Meyer, G., Gross, L., Organometàl.lics i Catàlisi Homogènia, Química Física i Inorgànica, and Universitat Rovira i Virgili

Subjects
Chemistry, Funcional de densitat, Teoria del, STM, Bdan, 1936-0851, Química, AFM
Abstract

Aiming to develop materials with new functionalities, we designed the synthesis of a naphthodiazaborinine (the BN isoster of the phenalenyl anion) that is bonded to a hindered di-orthosubstituted aryl system (9-anthracene). We used atomic force microscopy (AFM) to verify the structure of the molecule synthesized. To determine it unambiguously, we planarized the originally nonplanar molecule by removing H atoms that cause steric hindrance.

Full Text
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