The seminal discovery in 1865 by Kekulé that benzene nucleus exists with cyclic skeleton is considered to be the beginning of aromatic chemistry. Since then, a myriad of cyclic molecules displaying aromatic property have been synthesized. Meanwhile, borazine (B3N3H6), despite the isostructural and isoelectronic relationships with benzene, exhibits little aromaticity. Herein, we report the synthesis of a 1,3,2,5-diazadiborinine (B2C2N2R6) derivative, a hybrid inorganic/organic benzene, and we present experimental and computational evidence for its aromaticity. In marked contrast to the reactivity of benzene, borazine, and even azaborinines previously reported, 1,3,2,5-diazadiborinine readily forms the adducts with methyl trifluoromethanesulfonate and phenylacetylene without any catalysts. Moreover, 1,3,2,5-diazadiborine activates carbon dioxide giving rise to a bicycle[2,2,2] product, and the binding process was found to be reversible. These results, thus, demonstrate that 1,3,2,5-diazadiborinine features both nucleophilic and electrophilic boron centres, with a formal B(+I)/B(+III) mixed valence system, in the aromatic six-membered B2C2N2 ring.

An isolable phenylborylene species supported by two oxazol-2-ylidene ligands was synthesized and structurally characterized. Computational studies revealed the presence of lone-pair electrons on the boron atom in this molecule; therefore, there are eight electrons around the three-coordinate boron center. The nucleophilic property was confirmed by the reactions with trifluoromethanesulfonic acid and [(thf)Cr(CO)5], which gave the corresponding conjugate acid and a chromium-borylene complex, respectively.

Biomimetic processes have attracted huge attention in recent years due to their significant applications in biomedical areas such as bone tissue engineering. In the present study, a biomimetic process was employed to form a nanocrystallite apatite coating on metal. A thin bone-like apatite layer was coated onto titanium (Ti) metals via an alkali pre-treatment. This was followed by immersion in a simulated body fluid. Analysis of the coating by thin film x-ray diffraction and scanning electron microscope has shown that the apatite layer grown in this way exhibits nanostructure and has similar stoichiometry to that of natural bone. It is observed that the thickness of the apatite layer increases as the immersion period increases. The growth kinetics and mechanism are also discussed. A cross-sectional study has also shown that a uniform coating of carbonate-containing apatite (hydroxyapatite) is firmly adhered on the Ti metal. The adhesion of the apatite layer on the Ti substrate was further confirmed by a shear test, which has shown an average value of 9.5 MPa. The bioactivity of the coating was finally examined by cell culturing experiments. The results have shown that the nanocomposite prepared using the present method possesses good mechanical properties and bioactivity.

The reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) 1 towards metal precursors and its coordination chemistry were comprehensively studied.

One-electron oxidation of organoboron L2PhB: 1 (L = oxazol-2-ylidene) afforded a dicationic diborane(6) species [L2PhB-BPhL2]·2X (X = OTf, BF4, AlCl4) 3, representing a new strategy to construct a B(sp(3))-B(sp(3)) covalent bond. Each boron atom in 3 is in the formal oxidation state +II, and tetracoordinate with a Ph group and two oxazol-2-ylidenes. The cyclic voltammetry of 3 shows irreversible reduction and oxidation. Indeed, two-electron reduction of 3 with potassium graphite (KC8) afforded 1, making a fully reversible 1 ↔ 3 redox system, whereas two-electron oxidation with AuCl produced a boronium [L2PhBCl]OTf 4. Moreover, the reactions of 3 with isonitrile derivatives RNC: under heating conditions gave a cyano-substituted boronium [L2PhBCN]BF4 5 and a 2-boranyl-indole derivative 6, depending on the substituent R. The proposed reaction mechanism involves a borinylium radical 1(•+) which is generated via a homolytic cleavage of the B-B bond of 3.