One-pot microwave-assisted synthesis of organotin Schiff bases: an optical and electrochemical study towards their effects in organic solar cells?
New Journal of Chemistry Pub Date: 2018-07-19 DOI: 10.1039/C8NJ02998A
Abstract
Four organotin compounds bearing Schiff bases were prepared via a multicomponent microwave-assisted reaction among 2-hydroxy-1-naphthaldehyde, 2-aminophenol derivatives and the corresponding diorganotin oxide (R2SnO, R = nBu or Ph), with high yields and a low economic/environmental impact. All of the compounds were fully characterized by NMR (1H, 13C, and 119Sn) spectroscopy, high-resolution mass spectrometry, X-ray diffraction, cyclic voltammetry, UV/Vis spectroscopy, and fluorescence spectroscopy. All of the compounds absorb in the visible region around 480–490 nm, close to the maximum solar emission, with an optical band gap of around 2.3 eV and low fluorescence quantum yields. According to the electrochemical study, they present LUMO values close to that of [6,6]-phenyl-C61-butyric acid methyl ester (PCBM-C60), a typical electron acceptor organic photovoltaic material. Based on this combined optical/electrochemical study and as it allows the preparation of homogeneous spun films, the n-butyltin complex with carboxylic acid was selected for the investigation of its possible photovoltaic properties in organic solar cells. Charge photogeneration was obtained only using this organotin compound as an electron acceptor material with poly(3-hexylthiophene, P3HT) (typical electron donor material) with an open circuit voltage of 300 mV, a short-circuit current density of 0.11 mA cm?2 and an efficiency of 5.2 × 10?3%. Despite the fact that the efficiency is much lower with respect to the reference device P3HT/PCBM-C60, this preliminary result suggests that, after chemical and device processing optimization, tin complexes with Schiff bases could be applied as electron acceptor materials in organic photovoltaic devices.
Recommended Literature
- [1] Enantiomeric helical TiO2 nanofibers modulate different peptide assemblies and subsequent cellular behaviors? Xu Jie,Deng Xu,Weili WeiRSC Adv., 2019,9, 29149-29153 10.1039/C9RA04660G
- [2] Excited state dynamics of symmetric and asymmetric Cr3(dpa)4Cl2 measured using femtosecond transient absorption spectroscopy? Chao-Han Cheng,Wen-Zhen Wang,Shie-Ming Peng,I-Chia ChenPhys. Chem. Chem. Phys., 2017,19, 25471-25477 10.1039/C7CP03968A
- [3] Distribution and ecological risk assessment of typical antibiotics in the surface waters of seven major rivers, China? Environ. Sci.: Processes Impacts, 2021,23, 1088-1100 10.1039/D1EM00079A
- [4] Excitable dynamics in the bromate–sulfite–ferrocyanide reaction J. Zagora,M. Vosla?,L. Schreiberová,I. SchreiberPhys. Chem. Chem. Phys., 2002,4, 1284-1291 10.1039/B110048C
- [5] Evidence of pre-micellar aggregates in aqueous solution of amphiphilic PDMS–PEO block copolymer? Domenico Lombardo,Gianmarco Munaò,Pietro Calandra,Luigi Pasqua,Maria Teresa CaccamoPhys. Chem. Chem. Phys., 2019,21, 11983-11991 10.1039/C9CP02195G
- [6] Elusive 2-aminofuran Diels–Alder substrates for a straightforward synthesis of polysubstituted anilines? Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. MarcosOrg. Biomol. Chem., 2013,11, 6546-6555 10.1039/C3OB41411F
- [7] Enantiomorphic symmetry breaking in crystallization of molten sodium chlorate? Martin R. Ward,Gary W. Copeland,Andrew J. AlexanderChem. Commun., 2010,46, 7634-7636 10.1039/C0CC02563A
- [8] Excellent energy storage performance in NaNbO3-based relaxor antiferroeic ceramics under a low electric field XuxinCheng,XiaomingChen,PengyuanFan 10.1007/s10832-022-00283-w
- [9] Fe3O4/FeS2 heterostructures enable efficient oxygen evolution reaction? Xingqun Zheng,Lele Song,Xin Feng,Li Li,Zidong WeiJ. Mater. Chem. A, 2020,8, 14145-14151 10.1039/C9TA13775K
- [10] Estimation of hydrogen sulfide from crude petroleum: a unique invention using a simple chemosensor? Shampa Kundu,Prithidipa SahooNew J. Chem., 2019,43, 12369-12374 10.1039/C9NJ02628B
Journal Name:New Journal of Chemistry
research_products
-
CAS no.: 89640-58-4