A New 'Off-On' System Based on Core-Substituted Naphthalene Diimide with Dimethylamine for Reversible Acid-Base Sensing.

A new 'Off-On' system designed and synthesised by functionalisation of a naphthalene diimide (NDI) core with dimethylamine produces 4,9-bis(dimethylamino)-2,7-dioctylbenzo[lmn][3,8]-phenanthroline-1,3,6,8-(2H,7H)-tetraone, abbreviated as DDPT (1). DDPT 1 was synthesised using a simple strategy, namely aromatic nucleophilic substitution using Br2 -NDI with dimethylamine at 110 °C. DDPT was characterized by 1 H and 13 C NMR spectroscopy, ESI mass spectrometry and elemental analysis. DDPT 1 was then used for optical studies through protonation of its dimethylamine core with trifluoroacetic acid (TFA), blue-shifting the absorption band from 600 nm to 545 nm in solution. Interestingly, the fluorescence of DDPT 1 is weak in solution with a quantum yield Φ=0.09, which is significantly enhanced to Φ=0.78 upon addition of TFA. The limit of detection (LOD) was determined to 2.77 nm. Furthermore, DDPT 1 can be used for naked eyed detection not only under UV light (365 nm) but also using visible light, as clear changes can be clearly seen upon addition of TFA. The binding constant of DDPT was calculated to 2.1×10-3  m-1 . Importantly, DDPT 1 showed reversible switching by alternative addition of acid (TFA) and base (triethylamine) without loss of activity. Immobilised on paper, DDPT 1 can be used for strip-test sensing in which the colour changes from blue to reddish when expose to TFA vapours and reverse in the presence of triethylamine vapours.

Self-assembled kanamycin antibiotic-inorganic microflowers and their application as a photocatalyst for the removal of organic dyes.

Construction of hybrid three-dimensional (3D) hierarchical nanostructures via self-assembly of organic and inorganic compounds have recently attracted immense interest from scientists due to their unique properties and promise in a large range of applications. In this article, hybrid flower structures were successfully constructed by self-assembly an antibiotic, kanamycin, with Cu2+. The flower-like morphology was observed by scanning electron microscopy, to be approximately 4 µm in diameter and about 10 nm in thickness. FTIR spectroscopy and X-ray diffraction confirmed the antibiotic-inorganic hybrid structure was uniform composition, and showed crystallinity due to ordered self-assembly. The hybrid flowers showed high photocatalytic activity towards degradation of methyl blue during 240 minutes under visible light irradiation. A possible mechanism of photocatalytic activity was also proposed, that exposes the inherent advantages in using antibiotic-inorganic hybrid flowers as photocatalysts, where self-assembly can be used to generate active, high surface area structures for photodegradation of pollutants.

Meet the Board of ChemistryOpen: Sheshanath†V. Bhosale.

Sheshanath V. Bhoslae received his PhD from Freie University Berlin (Germany) in supramolecular chemistry under the supervision of Prof. J. H. Fuhrhop in 2004. He then pursued his postdoctoral studies with Prof. S. Matile at University of Geneva (Switzerland) under the auspices of a Roche Foundation Fellowship. This was followed by a stay at Monash University (Australia) for 5 years as an ARC-APD Fellow. He worked at RMIT University, Melbourne (Australia) for 6 years as ARC-Future Fellowship. Currently, Prof. Bhosale is working at the Department of Chemistry, Goa University (India) as a UGC-FRP Professor, His research interests lie in the design and synthesis of π-functional materials, especially small molecules, for sensing, biomaterials, and supramolecular chemistry applications. So far, Prof. Bhosale has produced 185 research articles and his work has been cited more than 4400 times, giving him an h-index of 32. He currently serves as an active Editorial Board member for ChemistryOpen.