A 3D stable Mn(II) metal-organic framework based on a flexible tetracarboxylate precursor and its photocatalytic properties

被引:14
作者
Wang, Jun [1 ]
Zhou, Dan [1 ]
Wang, Guang-Li [1 ]
Lu, Lu [1 ]
Pan, Ying [2 ]
Singh, Amita [3 ]
Kumar, Abhinav [3 ]
机构
[1] Sichuan Univ Sci & Engn, Sch Chem & Pharmaceut Engn, Zigong, Peoples R China
[2] Guangdong Med Univ, Dongguan Key Lab Drug Design & Formulat Technol, Key Lab Res & Dev New Med Mat, Sch Pharm, Dongguan 523808, Peoples R China
[3] Univ Lucknow, Fac Sci, Dept Chem, Lucknow 226007, Uttar Pradesh, India
关键词
Photocatalysis; Tetracarboxylate; Topology; DOS; HYDROTHERMAL SYNTHESIS; COORDINATION POLYMERS; DYE X3B; DEGRADATION; PHOTOLUMINESCENCE; POLYOXOMETALATE; NITROAROMATICS; ZN(II); ACID; FE3+;
D O I
10.1016/j.ica.2019.04.020
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A new metal-organic framework of [Mn-4(L)(2)(4,4'-bipy)(2)(H2O)(4)]center dot(H2O)(4,4'-bipy)] (1) has been synthesized using a symmetrical tetracarboxylate 5-[bis(4-carboxybenzyl)-amino] isophthalic acid (H4L) and 4,4'-bipyridine (4,4'-bipy) coligands. The single crystal X-ray diffraction study indicates that in 1, the Mn(II) centers are bridged by L4- and 4,4'-bipy ligands to furnish a 3D framework with a rare (4,6,6)-connected (4.5(3).6(2))(2)(4(2).5(4).6(6).7(2).8} {5(7).6(6).8(2)} topology. 1 exhibits related lower photocatalytic activity for degradation of organic dye methyl violet (MV) under UV light and offers good stability after performing photocatalysis. A mechanism for the photcatalytic property of MOF is proposed, which is based on the results of density of states (DOS) and partial DOS calculations.
引用
收藏
页码:186 / 191
页数:6
相关论文
共 66 条
[1]  
ADDISON W, 2008, J CHEM SOC DA, V29, P839
[2]  
BARNETT SA, 1998, CHEM COMMUN, V17, P1837
[3]   Fast photocatalytic degradation of rhodamine B over [Mo6Br8(N3)6]2- cluster units under sun light irradiation [J].
Barras, Alexandre ;
Cordier, Stephane ;
Boukherroub, Rabah .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2012, 123 :1-8
[4]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[5]   Inorganic crystal engineering using self-assembly of tailored building-blocks [J].
Blake, AJ ;
Champness, NR ;
Hubberstey, P ;
Li, WS ;
Withersby, MA ;
Schröder, M .
COORDINATION CHEMISTRY REVIEWS, 1999, 183 :117-138
[6]   Self-assembly of infinite double helical and tubular coordination polymers from Ag(CF3SO3) and 1,3-bis(4-pyridyl)propane [J].
Carlucci, L ;
Ciani, G ;
vonGudenberg, DW ;
Proserpio, DM .
INORGANIC CHEMISTRY, 1997, 36 (18) :3812-3813
[7]  
CARLUCCI L, 1999, CHEM COMMUN, V183, P117
[8]   Solvent-dependent 44 square grid and 64.82 NbO frameworks formed by Cu(Pyac)2 (bis[3-(4-pyridyl)pentane-2,4-dionato]copper(II)) [J].
Chen, BL ;
Fronczek, FR ;
Maverick, AW .
CHEMICAL COMMUNICATIONS, 2003, (17) :2166-2167
[9]   Towards the use of metal-organic frameworks for water reuse: a review of the recent advances in the field of organic pollutants removal and degradation and the next steps in the field [J].
Dias, Elton M. ;
Petit, Camille .
JOURNAL OF MATERIALS CHEMISTRY A, 2015, 3 (45) :22484-22506
[10]   Polyoxometalate-based materials for efficient solar and visible light harvesting: application to the photocatalytic degradation of azo dyes [J].
Dolbecq, Anne ;
Mialane, Pierre ;
Keita, Bineta ;
Nadjo, Louis .
JOURNAL OF MATERIALS CHEMISTRY, 2012, 22 (47) :24509-24521