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. Author manuscript; available in PMC: 2024 May 1.
Published in final edited form as: Chem Soc Rev. 2019 Mar 4;48(5):1362–1389. doi: 10.1039/c8cs00155c

Table 2.

Summary of porosity and functionality in single-component and permanently porous HOFs (until October 2018)

Types HOFs Formula Void/% Pore size/Å SBET/m2 g−1 Functionality Ref.
DAT derivatives HOF-1a C37H32N20 42 ~8.2 359 C2H2/C2H4 (56/3.9)e 28
HOF-2a C36H34N20O2 54.3 ~4.8 238 Separation of chiral secondary alcohols 138
HOF-3a C33H27N15 75 b7 165 C2H2/CO2 (47/21)e 133
HOF-4a C61H48N20 42.5 3.8 × 8.1 312 C2H4/C2H6 (11/3.6)e 117
HOF-5a C38H32N20 41.1 ~3.9 × 5.5, × 3.9 × 6.8 1101 CO2/CH4 (90/—)e, CO2/N2, and C2H2/CH4 (102/—)e 130
HOF-6a C56H42N24 63.4 ~6.4, ~7.5 130 Proton conduction, CO2/N2 145
HOF-7a C56H42N24OZn 3.2 × 4.7, 4.2 × 6.7 124 CO2/N2 (11/—)e 131
HOF-9a C56H42N24OZn 3.2 × 4.7, 4.2 × 6.7 124 Py/BTX, CO2/N2 (40/6)e 132
HOF-lOa C56H42N24OZn 55 3.2 × 4.7, 4.2 × 6.7 187 Fluorescence Ag+ sensing 154
Carboxylic acid IISERP-HOF1 C21H15NO6 ~34 9.1 × 9.4a 412 CO2/N2 (65/—)e 121
HOF-11 33.2 6.2 × 6.8 687 CO2/CH4, CO2/N2 (30/2)e, and C2H2/CH4 (45/8)e 123
Tcpb/H3BTB C27H18O6 38 18.5c 1095 CO2 and H2 adsorption 134
HOF-BTB 12/16.6c 955 C2H2/CH4 (64/8.7)e, C2H4/CH4, and C2H6/CH4 136
HOF-TCBP C40H26O8 56 17.8 × 26.3 2066 C3/CH4 and CH4/CH4 112
PFC-1/H4TBAPy C44H26O8 18 × 23 2122 Chemo-photodynamic therapy 115
CoTCPp C72H44N4O12Co ~19 4.0 × 6.5 98 Alkylbenzene oxidation 160
TCF-1 C29H20O8 17.3 2.9 × 5.5 to 4.2 × 6.4 CO2, CH4, and C6H6 adsorption 119
Tp-1 C60H36O12 54 ~11, 15.8a 788 Fluorescence and hydrocarbon 97
T12–1 C66H36O12 41 ~11, 4.6 × 15.8a 557 adsorption
T18–1 C72H36O12 58 ~11, 7.1 × 15.8a
Ex-1 C90H48O12 59 ~11, 11.4 × 15.8a
TpMe-1 C72H60O12 45.2 6.4 561 Fluorescence 151
TpF-1 C60H24F12O12 50.4 14.5 219
CPHAT-1a C72H44N4O12 31 6.4 649b Fluorescence 98
CBPHAT-la C72H44N4O12 45 14.5 1288 Fluorescence 99
PETHOF-1 C62H38O12 80 ~11c 1150 CO2/CH4 (32.6/10.6)e 85
PETHOF-2 C62H38O12 49 ~11c 1140 CO2/CH4 (43.4/4.2)e
Azole derivatives Trispyrazole 1 C33H12F12N6 56 16.5 1159 Fluorocarbon and hydrocarbon adsorption 88
Trispyrazole 16 C30H9F12N9 18 903 103
Tristetrazole 23 C27H6F12N12 11.9 222
Trispyrazole 25 C51H12F24N6 58.1 26.4 1821
Benzotrisimidazole C12H3F9N6 21.7 2.9 × 4.6 131 O2/Ar, O2/N2 137
FDM-15 C23H14N6 b11.5 749 p-Xylene/C8H10, C60 capture 139
Amide derivatives TTBI C23H14N6O3 60 14.5, 3.8 × 5.8 2796 CO2 and H2 adsorption 52
T2-β C23H14N6O3 1665 CH4 storage, C3H8/CH4 53
T2-γ C23H14N6O3 19.9 3425
T2-δ C23H14N6O3 365
NPSU-3 C46H60N6O5 16.1 10.8 29 Organic dyes adsorption 144
Pyridine derivatives HOF-8 C24H18N6O3 24 4.5 × 6.8 CO2/N2, CO2/H2 and C6H6 adsorption 91
SOF-1a C60H36N10 34 ~7.8 474 CO2 and C2H2 adsorption 51
Benzoin Cyclotetrabenzoin C32H24O8 10 42 CO2 and H2 adsorption 118
Porous molecular CB[6] (C36H36N24O12) 2H2O 14.4 6 210 C2H2 adsorption 70
solids TTP C18H12N3O6P3 25 4.6 240d 59 CO2 and CH4 adsorption 58
CC3 C72H84N12 5.8, 7.2 624 CO2, CH4 and H2 adsorption 72
TBC[4]DHQ C38H44O6 2.2, 11.2 230 CO2 adsorption 67
a

Distance of atom centers including vdW radii.

b

Estimated by PLATON.

c

Pore size distribution from 77 K N2.

d

Langmuir surface area.

e

The adsorption amount (cm3 g−1) at room temperature and 1 bar is presented in parentheses.