2021
DOI: 10.1007/s11814-020-0692-1
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Synthesis and use of new porous metal complexes containing a fusidate moiety as gas storage media

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Cited by 6 publications
(6 citation statements)
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“…The surface morphology of the Schiff bases was similar in terms of pore size and shape. The pore dimension was found to be in the range of 33.6-41.7 nm for 1, 29.5-39.0 nm for 2, and 24.9-53.7 nm for 3, which are comparable with those of telmisartan tin complexes (20-50 nm) [43] and fusidate metal complexes (29-50 nm) [45] and smaller than those of carvedilol metal complexes (51-394 nm) [42], melamine Schiff bases (20-392 nm) [46], polysilicates (35-208 nm) [47], and polyphosphates (28-981 nm) [48,49].…”
Section: Sem Of 1-3mentioning
confidence: 61%
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“…The surface morphology of the Schiff bases was similar in terms of pore size and shape. The pore dimension was found to be in the range of 33.6-41.7 nm for 1, 29.5-39.0 nm for 2, and 24.9-53.7 nm for 3, which are comparable with those of telmisartan tin complexes (20-50 nm) [43] and fusidate metal complexes (29-50 nm) [45] and smaller than those of carvedilol metal complexes (51-394 nm) [42], melamine Schiff bases (20-392 nm) [46], polysilicates (35-208 nm) [47], and polyphosphates (28-981 nm) [48,49].…”
Section: Sem Of 1-3mentioning
confidence: 61%
“…The specific surface areas of 1-3 were low, with Schiff base 1 with a meta arrangement (Figure 8) exhibiting the highest surface area (20.3 m 2 /g). The surface areas of trimethoprim Schiff bases (4.2-20.3 m 2 /g) were relatively larger than those of carvedilol metal complexes (6.1-9.0 m 2 /g) [42], melamine Schiff bases (5.2-11.6 m 2 /g) [46], and polysilicates (8.2-18.0 m 2 /g) [47], albeit smaller than those of telmisartan tin complexes (32.4-130.4 m 2 /g) [43], valsartan metal complexes (16.0-22.8 m 2 /g) [44], fusidate metal complexes (31.2-46.9 m 2 /g) [45], and polyphosphates (24.8-213.5 m 2 /g) [48,49].…”
Section: N 2 Isotherms Surface Area Pore Size Distribution Of 1-3mentioning
confidence: 92%
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