[1] Cui Y J, Yue Y F, Qian G D, Chen B L. Luminescent functional metal organic frameworks[J]. Chemical Reviews, 2012, 112:1126-1162.
[2] D'Andrade B W,Forrest S R. White organic light-emitting devices for solid-state lighting[J]. Advanced Materials, 2004, 16:1585-1595.
[3] Kent C A, Mehl B P, Ma L Q, Papanikolas J M, Meyer T J, Lin W B.Energy transfer dynamics in metal-organic frameworks[J]. Journal of the American Chemical Society, 2010, 132:12767-12769.
[4] Liu M,Quah H S, Wen S C, Yu Z S,Vittal J J,Ji W. Efficient third harmonic generation in a metal-organic framework[J]. Chemistry of Materials, 2016, 28:3385-3390.
[5] Zhou T H, Du Y H,Borgna A, Hong J D,Wang Y B, Han J Y, Zhang W, Xu R. Post-synthesis modification of a metal-organic framework to construct a bifunctionalphotocatalyst for hydrogen production[J]. Energy & Environmental Science, 2013, 6:3229-3234.
[6] Meng W, Xu Z Q, Ding J, Fan Y T. A systematic research on the synthesis, structures, and application in photocatalysis of cluster-based coordination complexes[J]. Crystal Growth & Design, 2014, 14:730-738.
[7] Zhao B, Chen X Y, Cheng P, Zong H J. Coordination polymers containing 1D channels as selective luminescent probes[J]. Journal of the American Chemical Society, 2004, 126:15394-15395.
[8] Fu Z,Chen Y, Zhang J, Liao S J. Correlation between the photoactive character and the structures of two novelmetal organic frameworks[J]. Journal of Materials Chemistry, 2011, 21:7895-7897.
[10] Mallick A, Garai B, Addicoat M A, Petkov P S, Heine T, Banerjee R.Solid state organic amine detection in aphotochromic porous metal organic framework[J]. Chemical Science, 2015, 6:1420-1425.
[11] Castellanos S, Goulet-Hanssens A, Zhao F, Dikhtiarenko A, Pustovarenko A, Hecht S,Gascon J,Kapteijn F,Bléger D. Structural Effects in Visible-light-responsive metal-organic frameworks incorporating ortho-fluoroazobenzenes[J]. European Journal of Medicinal Chemistry, 2016, 22:746-752.
[12] Park J, Jiang Q, Feng D, Zhou H C.Controlled generation of singlet oxygen in living cells with tunable ratios of the photochromic switch in metal-organic frameworks[J]. Angewandte Chemie International Edition, 2016, 55:7188-7193.
[13] Klán P,Wirz J. Photochemistry of Organic Compounds:From Concepts to Practice[M]. Chichester:Wiley,2009.
[14] Basa P N, AntalaS, Dempski R E, Burdette S C. A zinc(Ⅱ) photocage based on a decarboxylation metal ion release mechanism for investigating homeostasis and biological signaling[J]. Angewandte Chemie International Edition, 2015, 54:13027-13031.
[15] Duan Y, Waerenborgh J C, Clemente-Juan J M, Gimenez-Saiz C, Coronado E. Light-induced decarboxylation in a photo-responsive iron-containing complex based on polyoxometalate and oxalato ligands[J]. Chemical Science, 2017, 8:305-315.
[16] Epling G A, Lopes A. Fragmentation pathways in the photolysis of phenylacetic acid[J]. Journal of the American Chemical Society, 1976, 98:2700-2704.
[17] Budac D, Wan P.Photodecarboxylation:mechanism and synthetics[J]. Journal of Photochemistry and Photobiology A, 1992, 67:135-166.
[18] Sobczak M, Wagner P J. Light-Induced Decarboxylation of(o-Acylphenyl) acetic Acids[J]. Organic Letters, 2002, 4:379-382.
[19] Neto B A D, Lapis A A M,Júnior E N D S, Dupont J.2,1,3-benzothiadiazole and derivatives:synthesis, properties, reactions, andapplications in light technology of small molecules[J]. European Journal of Organic Chemistry, 2013, 2:228-255.
[20] Neto B A D,Carvalho P H P R, Correa J R. Benzothiadiazole derivatives as fluorescence imaging probes:beyond classical scaffolds[J]. Accounts of Chemical Research, 2015, 48:1560-1569.
[21] Eddaoudi M, Li H, YaghiO M, Highly Porous and stable metal-organic frameworks:structuredesign and sorption properties[J]. Journal of the American Chemical Society, 2000, 122:1391-1397.
[22] Agneeswari R,Tamilavan V, Song M, Hyun M H. Property modulation of benzodithiophene-based polymers via the incorporation of a covalently bonded novel 2,1,3-benzothiadiazole-1,2,4-oxadiazole derivative in their main chain for polymer solar cells[J]. Journal of Materials Chemistry C, 2014, 2:8515-8524.
[23] Sheldrick G M. SHELXS 97, Program for the Refinement of Crystal Structures[M].Germany:University of G ttingen, 1997.
[24] Sheldrick G M. SHELXS 97, Program for the Solution of Crystal Structures[M].Germany:University of G ttingen, 1997.
[25] Vooren A V, Prof J S K, Dr J C. Intrachain versus interchain electron transport in poly(fluorene-alt-benzothiadiazole):a quantum-chemical insight[J]. ChemPhysChem, 2008, 9:989-993.
[26] Watanabe M, Goto K, Fujitsuka M, Tojo S, Majima T, Shinmyozu T. 2,1,3-Benzothiadiazole dimers:preparation, structure,and transannular electronic interactions of syn-and anti-[2.2] (4,7) benzothiadiazolophanes[J]. Bulletin of the Chemical Society of Japan, 2010, 83:1155-1161.
[27] Cheng Q,Han X, Tong Y, Huang C, Ding J, Hou H W.Two 3D Cd(Ⅱ) metal-organic frameworks linked by benzothiadiazole dicarboxylates:fantastic S@Cd6 cage,benzothiadiazole antidimmer, and dual emission[J]. Inorganic Chemistry, 2017, 56:1696-1705. |