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. 2023 Nov 11;4(1):59–90. doi: 10.1021/acsorginorgau.3c00033

Table 8. Summary of Atmospheric CO2 Fixation over MOFsa.

Sr. No. MOF Reactive site Reactant Product Reaction conditions Ref
1 (I)Meim-UiO-66 Zr4+, I ECH 4-(chloromethyl)-1,3-dioxolan-2-one 0.1 MPa, 120 °C, 24 h (248)
2 MIL-IL(A) Cr3+, Br SO 4-phenyl-1,3-dioxolan-2-one 2 MPa, 110 °C, 2 h (325)
  MIL-IL(B)          
3 MIL-IMAc-Br Cu2+-COOH, Br ECH 4-(chloromethyl)-1,3-dioxolan-2-one 0.5 MPa, 60 °C, 24 h (81)
4 Mg-MOF-74 Mg2+, Co2+, OH SO 4-phenyl-1,3-dioxolan-2-one 2 MPa, 100 °C, 4 h (326, 327)
  Co-MOF-74          
5 UiO-66-NH2 Zr4+, NH2 SO 4-phenyl-1,3-dioxolan-2-one 2.0 MPa, 100 °C, 4 h (328)
6 BIT-101 Zn2+, COO PO 4-methyl-1,3-dioxolan-2-one 3 MPa, 160 °C, 24 h (329)
  BIT-102          
  BIT-103          
7 1-NH2 CONH, NH2 ECH, PO 4-(chloromethyl)-1,3-dioxolna-2-one-4-methyl-1,3-dioxolan-2-one 0.1 MPa, 90 °C, 50 h, 3 MPa, 100 °C, 6 h (330)
8 UMCM-1-NH2 Zn4O, NH2 PO 4-methyl-1,3-dioxolan-2-one 1.2 MPa, 120 °C, 24 h (331)
9 Zn-TATAB Zn2+, NH ECH 4-(chloromethyl)-1,3-dioxolan-2-one 1 atm, 100 °C, 16 h (332)
10 Co/Ni-TATAB Co2+, Ni2+, NH ECHECH 4-(chloromethyl)-1,3-dioxolan-2-one 1 bar, 80 °C, 15 h (279)
11 Zn-BTC-2MeIm Zn2+, 2MeIm ECH, PO 4-(chloromethyl)-1,3-dioxolan-2-one 3.0 MPa, 100 °C, 6 h (333)
12 Co(tp)(bpy) MOF-508a Co2+, Zn2+, free pyridine N ECH 4-(chloromethyl)-1,3-dioxolan-2-one 1 MPa, 100 °C, 8 h (334)
13 (Me2NH2)2·[Zn8(Ad)4(DABA)6O]·7DMF}n Zn2+, Ad, and NH2 ECH 4-(chloromethyl)-1,3-dioxolan-2-one 1 bar, 100 °C, 24 h (335)
14 ZIF-8 Zn2+, Im ECH 4-(chloromethyl)-1,3-dioxolan-2-one 7 bar, 100 °C, 4 h (336)
15 ZIF-90 Zn2+, CHO PO 4-methyl-1,3-dioxolan-2-one 2 MPa, 120 °C, 8 h (337)
16 CZ-ZIF Zn2+/Co2+, HmIm ECHPO 4-(chloromethyl)-1,3-dioxolan-2-one 7 bar, 100 °C, 4 h (338)
17 ZIF-67 Co2+, HmIm ECHPO 4-(chloromethyl)-1,3-dioxolan-2-one 10 bar, 120 °C, 6 h (339)
18 Ti-ZIF Ti4+, Im SO 4-phenyl-1,3-dioxolan-2-one 1.72 bar, 100 °C, 8 h (340)
19 MIL-101-P(n-Bu)3BrMIL-101-N(n Bu)3Br Cr3+, Br POPO 4-methyl-1,3-dioxolan-2-one 2.0 MPa, 80 °C, 8 h (341)
20 F-ZIF-90 Zn2+, I AGE 4-((allyloxy)methyl)-1,3-dioxolan-2-one 1.17 MPa, 120 °C, 6 h (342)
21 IL-ZIF-90 Zn2+, I PO 4-methyl-1,3-dioxolan-2-one 1.0 MPa, 120 °C, 3 h (343)
22 ZnTCPP⊂(Br)Etim-UiO-66 Zn2+, Br AGE 4-((allyloxy)methyl)-1,3-dioxolan-2-one 1 bar, 140 °C, 14 h (344)
23 Salen-Co(23%)⊂(Br)Etim-UiO- 66 Co3+, Br SO 4-phenyl-1,3-dioxolan-2-one 0.1 MPa, 120 °C,12 h (345)
24 UiO-67-IL Zr4+, Br ECH 4-(chloromethyl)-1,3-dioxolan-2-one 1 atm, 90 °C, 12 h (346)
25 FJI-C10 Cr3+, Br ECH 4-(chloromethyl)-1,3-dioxolan-2-one 1 bar, 80 °C, 12 h (347)
26 IL@MIL101-SO3H(4) Cr3+, Br ECH 4-(chloromethyl)-1,3-dioxolan-2-one 1 atm, 90 °C, 24 h (348)
27 MIL-101-IMBr-6 Cr3+, Br PO 4-methyl-1,3-dioxolan-2-one 0.8 MPa, 80 °C, 4 h (349)
28 IL/MIL-101-NH2 -COOH, NH2 PO 4-methyl-1,3-dioxolan-2-one 1.3 MPa, 120 °C, 1 h (350)
29 polyILs@MIL-101 Cr3+, Br SO 4-phenyl-1,3-dioxolan-2-one 1 bar, 70 °C, 48 h (351)
30 MIL-101-IP Cr3+, Br PO 4-methyl-1,3-dioxolan-2-one 1 atm, 25 °C, 48 h (352)
31 IL@ZIF-8(Zn/Co) Zn2+, Co2+, Br SO 4-phenyl-1,3-dioxolan-2-one 1 atm, 100 °C, 24 h (353)
32 F-IRMOF-3-2d Zn4O, -NH2, I POPOPO 4-methyl-1,3-dioxolan-2-one 2 MPa, 140 °C, 1.5 h (354)
  F-IRMOF-3-4d          
  F-IRMOF-3-6d          
33 F-IRMOF-3(MeI) Zn-OH, I AGE 4-((allyloxy)methyl)-1,3-dioxolan-2-one 1.2 MPa, 120 °C, 6 h (355)
  F-IRMOF-3(BuI)          
34 MIL-101-tmzOH-Br Cr3+, OH, Br ECH 4-(chloromethyl)-1,3-dioxolan-2-one 1 MPa, 80 °C, 2 h (356)
35 2MeIm@Co-BTC-x Co2+, MeIm ECHECH 4-(chloromethyl)-1,3-dioxolan-2-one 3.0 MPa, 90 °C, 5 h, 3.0 MPa, 90 °C, 7 h (357)
36 Cr-MIL-101-[BuPh3P]Br Cr3+, Br ECH 4-(chloromethyl)-1,3-dioxolan-2-one 1 MPa, 80 °C, 2 h (358)
37 [TMPyPMn(I)]4+(I)4@ZIF-8 Zn2+, Mn2+, I ECH 4-(chloromethyl)-1,3-dioxolan-2-one 1 bar, 100 °C, 36 h (359)
38 [Zn(II)NMeTPyP]4+[I]4@PCN- 224 Zn2+, I ECHPO 4-(chloromethyl)-1,3-dioxolan-2-one-4-methyl-1,3-dioxolan-2-one 0.8 MPa, 90 °C, 24 h (360)
a

Abbreviations: ECH = epichlorohydrin; PO = propylene oxide; SO = styrene oxide; AGE = allyl glycidyl ether; dhtp = 2,5-dihydroxyterephthalate; NH2-BDC = 2-aminoterephthalate; aip = 5-aminoisophthalic acid; NIP = 5-nitroisophthalic acid; L = N4,N4′-di(pyridine-4-yl) biphenyl-4,4′-dicarboxamide; Im = imidazole; BTC = 1,3,5-benzene tricarboxylate; HmIm = 2-methylimidazole; ICA = imidazole 2-carboxaldehyde; TATAB = 4,4′,4″-s-triazine-1,3,5-triyl-tri-p-aminobenzoic acid; DABCO = 1,4-diazabicyclo[2.2.2]-octane; MIL = Materials Institute Lavoisier; UiO = University of Oslo; BIT = Beijing Institute of Technology; Hip = 5-hydroxyisophthalic acid; Bpy = 4,4′-bipyridine; BTB = 1,3,5-tris(4-carboxyphenyl)benzene; DMF = N,N′-dimethylformamide; Ad = adeninate; DABA = 2,2′-dimethyl- 4,4′-azobenzoate; 2-MeIm = 2-methylimidazole; ZIF = zeolitic imidazolate framework; 2-F-BIM = 2-(furan-2-yl)-1H-benzo[d]imidazole; TCPP = 5,10,15,20-tetrakis(4-carboxyphenyl)porphyrin; IL = ionic liquid; ICA = imidazole-2-carboxyaldehyde; Etim = ethyl imidazolium; polyILs = poly(ionic liquids); IP = ionic polymer; MeI = methyl iodide; BuI = butyl iodide; IRMOF = isoreticular metal–organic framework; IMAc = 1H-imidazole-1-acetic acid; PCN = Porous coordination network; Zn(II)NMeTPyP = 5,10,15,20-tetrakis(1-methylpyridinium-4-yl) zinc(II) porphyrin; [(Etim-H2BDC)+(Br)] = 2-(3-ethyl-imidazol-1-yl)-terephthalic acid; ImBDC = 2-(imidazole-1-yl)terephthalate; salen-Co(III) - N,N′-bis(3-carboxylsalicylidene)-1,2-cyclohexanediamino cobalt(III) acetate; [BuPh3P]Br = 4-(bromobutyl)triphenylphosphonium bromide; MPImBr = 1-methyl-3-propylimidazolium bromide; HmIm = 2-methylimidazole; 2-Br-BDC = 2-bromoterephthalate; L = (Br) allylium-2-bp functionalized biphenyl dicarboxylic acid.