Non-covalent Interactions in the Synthesis and Design of New by Abel M. Maharramov, Kamran T. Mahmudov, Maximilian N.

By Abel M. Maharramov, Kamran T. Mahmudov, Maximilian N. Kopylovich, Armando J. L. Pombeiro

This booklet goals to review the position of non-covalent interactions, resembling hydrogen and halogen bonding, π-π, π-anion and electrostatic interactions, hydrophobic results and van der Waals forces within the synthesis of natural and inorganic compounds, in addition to in layout of latest crystals and serve as fabrics. The proposed e-book may still permit to mix, in a scientific means, fresh advances at the software of non-covalent interactions in synthesis and layout of recent compounds and practical fabrics with value in Inorganic, natural, Coordination, Organometallic, Pharmaceutical, organic and fabric Chemistries. accordingly, it may current a multi- and interdisciplinary personality assuring a slightly huge scope. We think it will likely be of curiosity to a variety of educational and learn employees about the synthesis of recent compounds, catalysis and fabrics. every one bankruptcy could be written by way of authors who're renowned specialists of their respective fields.

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Res. 2013, 46, 280. C. J. Allpress, L. M. Berreau, Coord. Chem. Rev. 2013, 257, 3005. 10. ‐J. Li, T. D. H. Bugg, Chem. Commun. 2005, 5, 130. 11. ‐J. Li, T. D. H. Bugg, Org. Biomol. Chem. 2007, 5, 507.  M. N. Kopylovich, K. T. Mahmudov, M. Haukka, A. J. L. Pombeiro, New J. Chem. 2014, 38, 495. 13. R. Solhnejad, F. S. Aliyeva, A. M. Maharramov, R. A. Aliyeva, F. M. Chyragov, A. V. Gurbanov, K. T. Mahmudov, M. N. Kopylovich, J. Mol. Struct. 2013, 1050, 180. 14. ‐B. Zhao, E. Bilodeau, V. Lemieux, A.

The great advantage of molecular hydrogen versus petroleum is its higher energy density that can be extracted with great efficiency without producing greenhouse gases. The impor­ tance of this fuel alternative is evidenced in the several reviews published over the years [138–143].

Thus, from now on, 1,2‐dihydro‐1,2‐azaborine will be commonly referred as azaborine. Despite many advances in azaborine chemistry, with many reported B‐ and N‐ substitutions [43], the parent compound, 1,2‐azaborine, had not been synthesized yet. That problem was only solved in 2009 by Liu et al. who reported its isolation, although in very low yields. Four years later, in 2013, Liu once again described a protection group‐free gram‐scale synthesis of compound 7, which finally allowed an exten­ sive characterization [45].

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