26
[1]
27
28
P. Bernardo, E. Drioli, G. Golemme, Membrane gas separation: A review/state of the art, Ind.
Eng. Chem. Res. 48 (2009) 4638–4663.
[2]
F. Wu, M.D. Argyle, P.A. Dellenback, M. Fan, Progress in O2 separation for oxy-fuel
29
combustion–A promising way for cost-effective CO2 capture: A review, Prog. Energy Combust.
30
Sci. 67 (2018) 188–205.
31
[3]
32
33
T. Burdyny, H. Struchtrup, Hybrid membrane/cryogenic separation of oxygen from air for use in
the oxy-fuel process, Energy. 35 (2010) 1884–1897.
[4]
H. Lin, M. Zhou, J. Ly, J. Vu, J.G. Wijmans, T.C. Merkel, J. Jin, A. Haldeman, E.H. Wagener, D.
34
Rue, Membrane-based oxygen-enriched combustion, Ind. Eng. Chem. Res. 52 (2013) 10820–
35
10834.
19
[5]
J.-G. Jee, J.-S. Lee, C.-H. Lee, Air Separation by a Small-Scale Two-Bed Medical O2 Pressure
Swing Adsorption, Ind. Eng. Chem. Res. 40 (2001) 3647–3658.
[6]
P.D. Southon, D.J. Price, P.K. Nielsen, C.J. McKenzie, C.J. Kepert, Reversible and selective O2
chemisorption in a porous metal-organic host material, J. Am. Chem. Soc. 133 (2011) 10885–
10891.
[7]
frameworks, Chem. Soc. Rev. 38 (2009) 1477–1504.
[8]
10
J.R. Li, R.J. Kuppler, H.C. Zhou, Selective gas adsorption and separation in metal-organic
J.-R. Li, J. Sculley, H.-C. Zhou, Metal–Organic Frameworks for Separation, Chem. Rev. 112
(2012) 869–932.
[9]
D.J. Xiao, M.I. Gonzalez, L.E. Darago, K.D. Vogiatzis, E. Haldoupis, L. Gagliardi, J.R. Long,
11
Selective, Tunable O2 Binding in Cobalt(II)-Triazolate/Pyrazolate Metal-Organic Frameworks, J.
12
Am. Chem. Soc. 138 (2016) 7161–7170.
13
[10]
14
15
D.F. Sava Gallis, M. V. Parkes, J.A. Greathouse, X. Zhang, T.M. Nenoff, Enhanced O2 selectivity
versus N2 by partial metal substitution in Cu-BTC, Chem. Mater. 27 (2015) 2018–2025.
[11]
L.J. Murray, M. Dinca, J. Yano, S. Chavan, F. Bonino, S. Bordiga, C.M. Brown, J.R. Long,
16
Highly-Selective and Reversible O2 Binding in Cr3(1,3,5-benzenetricarboxylate)2, J. Am. Chem.
17
Soc. 132 (2010) 7856–7857.
18
[12]
W. Zhang, D. Banerjee, J. Liu, H.T. Schaef, J. V. Crum, C.A. Fernandez, R.K. Kukkadapu, Z.
19
Nie, S.K. Nune, R.K. Motkuri, K.W. Chapman, M.H. Engelhard, J.C. Hayes, K.L. Silvers, R.
20
Krishna, B.P. McGrail, J. Liu, P.K. Thallapally, Redox-Active Metal-Organic Composites for
21
Highly Selective Oxygen Separation Applications, Adv. Mater. 28 (2016) 3572–3577.
22
[13]
E.D. Bloch, L.J. Murray, W.L. Queen, S. Chavan, S.N. Maximoff, J.P. Bigi, R. Krishna, V.K.
23
Peterson, F. Grandjean, G.J. Long, B. Smit, S. Bordiga, C.M. Brown, J.R. Long, Selective
24
binding of O2 over N2 in a redox-active metal-organic framework with open iron(II) coordination
25
sites, J. Am. Chem. Soc. 133 (2011) 14814–14822.
26
[14]
T. Zhao, X. Zhang, Z. Tu, Y. Wu, X. Hu, Low-viscous diamino protic ionic liquids with fluorine-
27
substituted phenolic anions for improving CO2 reversible capture, J. Mol. Liq. 268 (2018) 617–
28
624.
29
[15]
J.F. Huang, H. Luo, C. Liang, D.E. Jiang, S. Dai, Advanced liquid membranes based on novel
30
ionic liquids for selective separation of olefin/paraffin via olefin-facilitated transport, Ind. Eng.
31
Chem. Res. 47 (2008) 881–888.
32
[16]
S. Seo, M. Quiroz-Guzman, M.A. Desilva, T.B. Lee, Y. Huang, B.F. Goodrich, W.F. Schneider,
33
J.F. Brennecke, Chemically tunable ionic liquids with aprotic heterocyclic anion (AHA) for CO2
34
capture, J. Phys. Chem. B. 118 (2014) 5740–5751.
20
[17]
S. Zeng, X. Zhang, L. Bai, X. Zhang, H. Wang, J. Wang, D. Bao, M. Li, X. Liu, S. Zhang, Ionic-
Liquid-Based CO2 Capture Systems: Structure, Interaction and Process, Chem. Rev. 117 (2017)
9625–9673.
[18]
overview and progress, Energy Environ. Sci. 5 (2012) 6668–6681.
[19]
L.Y. Wang, Y.L. Xu, Z.D. Li, Y.N. Wei, J.P. Wei, CO2/CH4 and H2S/CO2 Selectivity by Ionic
Liquids in Natural Gas Sweetening, Energy and Fuels. 32 (2018) 10–23.
[20]
10
X. Zhang, X. Zhang, H. Dong, Z. Zhao, S. Zhang, Y. Huang, Carbon capture with ionic liquids:
F. Karadas, M. Atilhan, S. Aparicio, Review on the use of ionic liquids (ILs) as alternative fluids
for CO2 capture and natural gas sweetening, Energy and Fuels. 24 (2010) 5817–5828.
[21]
11
T. Torimoto, T. Tsuda, K.I. Okazaki, S. Kuwabata, New frontiers in materials science opened by
ionic liquids, Adv. Mater. 22 (2010) 1196–1221.
12
[22]
R.D. Rogers, K.R. Seddon, Ionic Liquids-Solvents of the Future?, Science. 302 (2003) 792–793.
13
[23]
R.L. Vekariya, A review of ionic liquids: Applications towards catalytic organic transformations,
14
15
J. Mol. Liq. 227 (2017) 44–60.
[24]
S. Kasahara, E. Kamio, H. Matsuyama, Improvements in the CO2 permeation selectivities of
16
amino acid ionic liquid-based facilitated transport membranes by controlling their gas absorption
17
properties, J. Memb. Sci. 454 (2014) 155–162.
18
[25]
19
20
applications of functionalised ionic liquids, Chem. A Eur. J. 12 (2006) 2122–2130.
[26]
21
22
Z. Fei, T.J. Geldbach, D. Zhao, P.J. Dyson, From dysfunction to bis-function: On the design and
E.D. Bates, R.D. Mayton, I. Ntai, J.H. Davis, CO2 capture by a task-specific ionic liquid, J. Am.
Chem. Soc. 124 (2002) 926–927.
[27]
D.E. Jiang, S. Dai, First principles molecular dynamics simulation of a task-specific ionic liquid
23
based on silver-olefin complex: Atomistic insights into a separation process, J. Phys. Chem. B.
24
112 (2008) 10202–10206.
25
[28]
P. Nockemann, B. Thijs, T.N. Parac-Vogt, K. Van Hecke, L. Van Meervelt, B. Tinant, I.
26
Hartenbach, T. Schleid, V.T. Ngan, M.T. Nguyen, K. Binnemans, Carboxyl-Functionalized Task-
27
Specific Ionic Liquids for Solubilizing Metal Oxides, Inorg. Chem. 47 (2008) 9987–9999.
28
[29]
29
30
I. Newington, J.M. Perez-Arlandis, T. Welton, Ionic liquids as designer solvents for nucleophilic
aromatic substitutions, Org. Lett. 9 (2007) 5247–5250.
[30]
F. Moghadam, E. Kamio, H. Matsuyama, High CO2 separation performance of amino acid ionic
31
liquid-based double network ion gel membranes in low CO2 concentration gas mixtures under
32
humid conditions, J. Memb. Sci. 525 (2017) 290–297.
33
[31]
34
35
36
S. Kasahara, E. Kamio, T. Ishigami, H. Matsuyama, Amino acid ionic liquid-based facilitated
transport membranes for CO2 separation, Chem. Commun. 48 (2012) 6903–6905.
[32]
H. Fu, X. Wang, H. Sang, R. Fan, Y. Han, J. Zhang, Z. Liu, The study of bicyclic amidine-based
ionic liquids as promising carbon dioxide capture agents, J. Mol. Liq. 304 (2020) 112805.
21
[33]
P. Mehta, S. Vedachalam, G. Sathyaraj, S. Garai, G. Arthanareeswaran, K. Sankaranarayanan,
Fast sensing ammonia at room temperature with proline ionic liquid incorporated cellulose
acetate membranes, J. Mol. Liq. 305 (2020) 112820.
[34]
T. Zhao, P. Li, X. Feng, X. Hu, Y. Wu, Study on absorption and spectral properties of H2S in
carboxylate protic ionic liquids with low viscosity, J. Mol. Liq. 266 (2018) 806–813.
[35]
A. Matsuoka, E. Kamio, T. Mochida, H. Matsuyama, Facilitated O2 transport membrane
containing Co(II)-salen complex-based ionic liquid as O2 carrier, J. Memb. Sci. 541 (2017) 393–
402.
[36]
A. Matsuoka, E. Kamio, H. Matsuyama, Investigation into the Effective Chemical Structure of
10
Metal-Containing Ionic Liquids for Oxygen Absorption, Ind. Eng. Chem. Res. 58 (2019) 23304–
11
23316.
12
[37]
Q. Zheng, S.J. Thompson, S. Zhou, M. Lail, K. Amato, A. V. Rayer, J. Mecham, P. Mobley, J.
13
Shen, B. Fletcher, Task-Specific Ionic Liquids Functionalized by Cobalt(II) Salen for Room
14
Temperature Biomimetic Dioxygen Binding, Ind. Eng. Chem. Res. 58 (2019) 334–341.
15
[38]
16
17
phosphonium ionic liquids as potential electrolytes, Electrochem. Commun. 9 (2007) 2353–2358.
[39]
18
19
K. Tsunashima, M. Sugiya, Physical and electrochemical properties of low-viscosity
H.T. Clarke, B. Gillespie, S.Z. Weisshaus, The Action of Formaldehyde on Amines and Amino
Acids, J. Am. Chem. Soc. 55 (1933) 4571–4587.
[40]
K.C. Gupta, H.K. Abdulkadir, S. Chand, Polymer-immobilized N,N′-
20
bis(acetylacetone)ethylenediamine cobalt(II) Schiff base complex and its catalytic activity in
21
comparison with that of its homogenized analogue, J. Appl. Polym. Sci. 90 (2003) 1398–1411.
22
[41]
M. Okuhata, T. Mochida, Ionic Liquids from the Cationic Cobalt(III) Schiff Base Complex,
23
[Co(acacen)L2][Tf2N] (acacen = N,N’ bis(acetylacetone)ethylenediamine, Tf2N =
24
bis(trifluoromethanesulfonyl)amide), J. Coord. Chem. 67 (2014) 1361–1366.
25
[42]
26
I. Canals, J.A. Portal, E. Bosch, M. Rosés, Retention of ionizable compounds on HPLC. 4.
Mobile-phase pH measurement in methanol/water, Anal. Chem. 72 (2000) 1802–1809.
27
[43]
Z. Lei, C. Dai, B. Chen, Gas solubility in ionic liquids, Chem. Rev. 114 (2014) 1289–1326.
28
[44]
B. Dębski, A. Hänel, R. Aranowski, S. Stolte, M. Markiewicz, T. Veltzke, I. Cichowska-
29
Kopczyńska, Thermodynamic interpretation and prediction of CO2 solubility in imidazolium
30
ionic liquids based on regular solution theory, J. Mol. Liq. 291 (2019).
31
[45]
M.S. Shannon, J.M. Tedstone, S.P.O. Danielsen, M.S. Hindman, A.C. Irvin, J.E. Bara, Free
32
volume as the basis of gas solubility and selectivity in imidazolium-based ionic liquids, Ind. Eng.
33
Chem. Res. 51 (2012) 5565–5576.
34
[46]
S. Seo, M.A. Desilva, H. Xia, J.F. Brennecke, Effect of Cation on Physical Properties and CO2
35
Solubility for Phosphonium-Based Ionic Liquids with 2-Cyanopyrrolide Anions, J. Phys. Chem.
36
B. 119 (2015) 11807–11814.
22
[47]
M.J. Carter, D.P. Rillema, F. Basolo, Oxygen Carrier and Redox Properties of Some Neutral
Cobalt Chelates. Axial and in-Plane Ligand Effects, J. Am. Chem. Soc. 96 (1974) 392–400.
[48]
A. Pui, I. Berdan, I. Morgenstern-Badarau, A. Gref, M. Perrée-Fauvet, Electrochemical and
spectroscopic characterization of new cobalt(II) complexes. Catalytic activity in oxidation
reactions by molecular oxygen, Inorganica Chim. Acta. 320 (2001) 167–171.
[49]
Ethylenebis(acetylacetoniminato)ligandcobalt (II), J. Am. Chem. Soc. 92 (1970) 55–60.
[50]
G. Amiconi, G., Brunori, M., Antonini, E., Tauzher, G., Costa, Thermodynamics of the
Reversible Oxygenation of Bis(Acetylacetone)-Ethylenediiminecobalt (II) in Pyridine, Nature.
10
11
A.L. Crumbliss, F. Basolo, Monomeric Oxygen Adducts of N,N’-
228 (1970) 549–551.
[51]
S. Patel, P. Patel, S.B. Undre, S.R. Pandya, M. Singh, S. Bakshi, DNA binding and dispersion
12
activities of titanium dioxide nanoparticles with UV/vis spectrophotometry, fluorescence
13
spectroscopy and physicochemical analysis at physiological temperature, J. Mol. Liq. 213 (2016)
14
304–311.
15
[52]
D. Kumar, A. Chandra, M. Singh, Effect of Pr(NO3)3, Sm(NO3)3, and Gd(NO3)3 on Aqueous
16
Solution Properties of Urea: A Volumetric, Viscometric, Surface Tension, and Friccohesity Study
17
at 298.15 K and 0.1 MPa, J. Solution Chem. 45 (2016) 750–771.
18
[53]
R. Chetty, M. Singh, In-vitro interaction of cerium oxide nanoparticles with hemoglobin, insulin,
19
and dsDNA at 310.15 K: Physicochemical, spectroscopic and in-silico study, Int. J. Biol.
20
Macromol. 156 (2020) 1022–1044.
21
[54]
22
23
C. Janiak, A critical account on n-n stacking in metal complexes with aromatic nitrogencontaining ligands, J. Chem. Soc. Dalt. Trans. (2000) 3885–3896.
[55]
M.K. Milčić, Z.D. Tomić, S.D. Zarić, Very strong metal ligand aromatic cation-π interactions in
24
transition metal complexes: Intermolecular interaction in tetraphenylborate salts, Inorganica
25
Chim. Acta. 357 (2004) 4327–4329.
26
[56]
H. Keypour, M. Shayesteh, M. Rezaeivala, F. Chalabian, Y. Elerman, O. Buyukgungor,
27
Synthesis, spectral characterization, structural investigation and antimicrobial studies of
28
mononuclear Cu(II), Ni(II), Co(II), Zn(II) and Cd(II) complexes of a new potentially hexadentate
29
N2O4 Schiff base ligand derived from salicylaldehyde, J. Mol. Struct. 1032 (2013) 62–68.
30
[57]
M.A.A.F. de, B. de Castro, A.M. Coelho, D. Domingues, C. Freire, J. Morais, Electrochemical
31
and structural studies of nickel(II) complexes with N2O2 Schiff base ligands derived from 2-
32
hydroxy-1-naphthaldehyde. Molecular structure of N,N′-2,3-dimethylbutane-2,3-diyl-bis(2-
33
hydroxy-1-naphthylideneiminate) nickel(II), Inorganica Chim. Acta. 205 (1993) 157–166.
34
[58]
A. Gutiérrez, M.F. Perpiñán, A.E. Sánchez, M.C. Torralba, M.R. Torres, Stabilization of the
35
cobalt coordination site in transmetalation processes on dinuclear salen derivatives, Inorganica
36
Chim. Acta. 363 (2010) 1837–1842.
23
[59]
C.A. Hunter, J.K.M. Sanders, The Nature of π-π Interactions, J. Am. Chem. Soc. 112 (1990)
5525–5534.
[60]
N. Mahata, A.R. Silva, M.F.R. Pereira, C. Freire, B. de Castro, J.L. Figueiredo, Anchoring of a
[Mn(salen)Cl] complex onto mesoporous carbon xerogels, J. Colloid Interface Sci. 311 (2007)
152–158.
[61]
the investigation of intramolecular π-stacking interactions, J. Org. Chem. 70 (2005) 2299–2305.
[62]
M.A. Muñoz, O. Sama, M. Galán, P. Guardado, C. Carmona, M. Balón, Hydrogen bonding NH/π
interactions between betacarboline and methyl benzene derivatives, Spectrochim. Acta - Part A
10
11
X. Mei, C. Wolf, Highly congested nondistorted diheteroarylnaphthalenes: Model compounds for
Mol. Biomol. Spectrosc. 57 (2001) 1049–1056.
[63]
A.H. Kianfar, L. Keramat, M. Dostani, M. Shamsipur, M. Roushani, F. Nikpour, Synthesis,
12
spectroscopy, electrochemistry and thermal study of Ni(II) and Cu(II) unsymmetrical N2O2 Schiff
13
base complexes, Spectrochim. Acta - Part A Mol. Biomol. Spectrosc. 77 (2010) 424–429.
14
[64]
15
16
CH3OH), Inorganica Chim. Acta. 141 (1988) 139–144.
[65]
17
18
E.M. Nour, A.A. Taha, I.S. Alnaimi, Infrared and Raman studies of [UO2(salen)(L)] (L=H2O and
M. Tsuboi, Y. Kyogoku, T. Shimanouchi, Infrared absorption spectra of protonated and
deprotonated nucleosides, Biochim. Biophys. Acta. 55 (1962) 1–12.
[66]
H. Shirota, T. Mandai, H. Fukazawa, T. Kato, Comparison between dicationic and monocationic
19
ionic liquids: Liquid density, thermal properties, surface tension, and shear viscosity, J. Chem.
20
Eng. Data. 56 (2011) 2453–2459.
21
22
[67]
S. Biradar, R. Kasugai, H. Kanoh, H. Nagao, Y. Kubota, K. Funabiki, M. Shiro, M. Matsui,
Liquid azo dyes, Dye. Pigment. 125 (2016) 249–258.
23
24
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