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Metal–organic framework (MOF)-derived nanostructures exhibit wonderful characteristics and possess broad application potential by modulating the complex composition and inner nanostructure. Although various MOF-based nanocomposites have been successfully developed, a facile method that can easily modulate the structure-dependent chemical components of the MOF-derived hybrids remains a challenge. By coating zeolitic imidazolate framework-8 (ZIF-8) with Au/polydopamine (Au/PDA) via in situ redox-oxidation polymerization of HAuCl4 and dopamine, it was found that the ZIF-8 templates were simultaneously etched off to give Au/PDA hybrid microcapsules with a cubic shape. This one-step sacrificial templating process followed a competing chelation between gold ions and Zn2+ cations to 2-methylimidazole and PDA; thus, both the hollow and the yolk-like hybrid cubic microcapsules were controllably obtained by varying the synthetic dynamics. Owing to the hollow nature, penetrated PDA shell, well-distributed Au nanocrystals, and unique stable nanostructure, the non-spherical Au/PDA hybrid cubic microcapsules showed high performance in catalyzing the reduction of 4-nitrophenol as well as adsorption/release of ibuprofen as a model drug. Moreover, this simple strategy offers a controllable design in developing multifunctional nanocomposites with definite inner nanostructures and activities for nanocatalysis, drug delivery, energy storage etc. [ABSTRACT FROM AUTHOR]

A mild and environmentally electrochemical method for the synthesis of quinazolines and quinazolinones has been developed through anodic oxidation decarboxylative of α-oxocarboxylic acids. The present reaction was efficiently conducted by using simple and cheap NH 4 I as the N-source and electrolyte in an undivided cell. The desired products, quinazolines and quinazolinones, were isolated in high yield under chemical oxidant free conditions., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

This work reports a hard self-template method to synthesize core/shell like Fe3O4@C microparticles, in which the Pd nanocrystals can be alternatively incorporated into the carbon shells. The Fe3O4@polyaniline core/shell microspheres were first synthesized as the precursor by in situ polymerization of aniline onto the surface of the Fe3O4 microspheres. In a subsequent carbonization of the precursor under a vacuum oven, the Fe3O4 core was preserved and the polyaniline shell transferred into carbon shells enveloping the magnetic sphere, forming magnetic Fe3O4@C microspheres. The Pd ions could be impregnated into the polyaniline shell, and thus the obtained composites were transformed into Fe3O4@C/Pd microspheres under the same vacuum heating progress. The as-obtained system demonstrates superparamagnetic characteristics, which would benefit its potential application in nanocatalysts. This strategy provides an efficient approach for tailoring core/shell materials with desired functionalities and structures by adjusting the precursors and structure-directing agents.