We report unprecedented phase stability of cubic CsPbBr 3 quantum dots in ambient air obtained by using Br 2 as halide precursor. Mechanistic investigation reveals the decisive role of temperaturecontrolled in situ generated, oleylammonium halide species from molecular halogen and amine for the long term stability and emission tunability of CsPbX 3 (X ¼ Br, I) nanocrystals.High photoluminescence quantum yield (PL QY), narrow emission linewidth, tunable band gap, large diffusion lengths and low exciton binding energies are some of the key attributes of all-inorganic caesium lead halide perovskite nanocrystals (LHP NCs) i.e., CsPbX 3 , X ¼ I, Br, This novel class of NCs has been shown to be highly "defect tolerant", i.e. defect states are either shallow or localized in the valence or the conduction band. 1,2 Unlike conventional semiconductor NCs, the rigorous passivation of their surface via formation of core/shell structures or other methods is not required to achieve high QY. These LHP NCs are promising building blocks for light emitting diode, 3,4 solar cell, 5,6 laser, 7 photocatalysis 8 and detector. 9 Despite the recent surge of studies on CsPbX 3 perovskite NCs, a persisting drawback is their poor phase stability in ambient air. For example, cubic (a) "black" phase CsPbI 3 (E g ¼ 1.73 eV) perovskite NCs undergo rapid phase transformation to nonluminescent orthorhombic (d) "yellow" phase in ambient condition ( Fig. S1 †) leading to undesired changes of the band gap, optical and electrical properties. 6,10,11 Similarly, cubic (a) CsPbBr 3 (E g ¼ 2.25 eV) is unstable at ambient condition. 12 For successful integration of these materials into devices, the issue of long-term phase stability must thus be addressed. 6,13 Most of the reported strategies involve the use of additives such as halide salt, 12 phosphinic acid, 14 ammonium halide, 11 2,2 0 -iminodibenzoic acid 15 sulphides and metal ions 16 and polymers 5 or via special post-synthetic purication step. 6,10 Herein, we report the rst synthesis of highly stable, cubic a-CsPbBr 3 perovskite NCs using Br 2 as an independent halide precursor. In a typical synthesis, lead acetate is dissolved in 1-octadecene in the presence of oleyl amine (OAm) and oleic acid (OA). To this solution, Br 2 (warning: handle the liquid Br 2 in fume hood, Br 2 vapors are toxic) and caesium oleate solutions (both dissolved in ODE) are sequentially added. Phase stability and emission colour tunability are achieved by controlling the reaction temperature (75-200 C) and amount of Br 2 (0.6-1.2 mmol) under air-free synthetic condition (cf. ESI; Experimental section †). The "three-precursor" nature 16-18 of our synthetic scheme allows for independent tuning of the amount of the individual elements viz., Cs + , Pb 2+ and X À ions and in turn, allows for the precise control over the surface chemistry. 17 Highly crystalline, monodisperse 7.62 AE 1.0 nm sized cubic a-CsPbBr 3 NCs (Fig. 1a) were synthesised under optimized conditions using Cs : Pb : Br 2 ratio of 1 : 1 : 6 at 200 C. Highresol...
Metal−organic frameworks (MOFs) are extensively used in catalysis due to their robust structure, well-defined periodic reaction centers, and high porosity. We report Cu 3 (BTC) 2 •(H 2 O) 3 (HKUST-1) as an efficient heterogeneous catalyst for aziridination of alkene and ring-opening reaction of activated aziridines. Furthermore, we demonstrate that the transfer of a nitrogen group from PhINTs to olefins and its analogue to give aziridines takes place at the coordinatively unsaturated Cu(II) site of Cu 3 (BTC) 2 −MOF; however, the ring opening of activated aziridines is controlled by the Cu(II) Lewis acid site, and generation of coordinative unsaturation by thermal activation of the MOF is not necessarily important. The key advantage of this catalytic approach is the direct formation of C−C, C−N, C−O, and C−S bonds yielding β-aryl sulfonamide derivatives through a simultaneous aziridination ring-opening reaction of the alkene in one pot using a single catalyst.
Lead halide perovskite (LHP) based colloidal quantum dots (CQDs) have tremendous potential for photocatalysis due to their exceptional optical properties.
The coordinatively unsaturated sites (CUS) are vital in metal-centered catalysis. Metal–organic frameworks (MOFs) provide a unique opportunity to generate and stabilize CUS due to their robust structure. Generally, the generation of CUS in MOFs needs prior activation under heat and high vacuum to remove labile molecules occupying the catalytic sites. Herein, we report a solvothermal synthesis of a ready-to-use copper MOF containing accessible pre-existing CUS that does not need activation. The single crystal X-ray diffraction structure reveals a square planar Cu(II) center with two N-methylimidazoles (Mim) and one benzenedicarboxylic acid (BDC) with the formula unit [CuII(BDC)(Mim)2] n (Cu-1D) forming an infinite one-dimensional (1D) chain along the c axis. The 1D chains are stabilized by noncovalent π–π, CH···π, and H-bonding interaction to give 2D (sheet-like) and 3D networks in the solid state. The quantification of non-covalent interaction is studied by Hirshfeld surface analysis, and the formation of a higher architecture in the solid state is confirmed by SEM analysis. The reported Cu-1D MOF acts as a solid heterogeneous catalyst and exhibits efficient catalytic activity in intermolecular and intramolecular cross-coupling reactions. Intermolecular C-heteroatom cross-coupling of a variety of N-heterocycles, aliphatic, aromatic, alicyclic amines and amides (C–N), phenols (C–O), and thiols (C–S) with aryl halides (halide = I, Br) was achieved with 70 to 95% yield, better than the state-of-the-art Cu-based homogenous system. The C–N coupling catalytic cycle is initiated by the in situ reduction of Cu(II) by KOH/DMSO to Cu(I) species. Subsequently, Cu(I) undergoes oxidative addition followed by reductive elimination to form a cross-coupled product. High stereoselectivity was found for the intramolecular C–N coupling reaction to give tetrahydroquinoxalines with an enantiomeric excess (ee) of more than 99%. For a broader application, Cu-1D was applied as the catalyst for the synthesis of a library of aziridines that gives yields of up to 99% with more than 93% recyclability for each cycle.
Two efficient, modular, step- and pot-economic strategies to access various 5,6,7,12-tetrahydrobenzo[2,3]azepino[4,5-b]indoles and 6,7-dihydro-5H-benzo[5,6][1,4]diazepino[1,7-a]indoles are disclosed that advance via S2-type regioselective ring opening of enantiopure aziridines with 2-(2-bromophenyl)-1H-indoles at their C3 and indolyl N centers, respectively, followed by Cu-mediated C-N cyclization which furnishes the products in excellent yields with outstanding enantiomeric excesses (up to >99%).
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