Literature DB >> 15381984

Guest sorption and desorption in the metal-organic framework [Co(INA)(2)] (INA=isonicotinate)--evidence of intermediate phases during desorption.

Qiang Wei1, Mark Nieuwenhuyzen, Frederick Meunier, Chris Hardacre, Stuart L James.   

Abstract

The metal-organic framework [Co(INA)(2)]x0.5EtOH (INA = isonicotinate, NC(5)H(4)-4-CO(2)(-)), was synthesised under solvothermal conditions. Its X-ray crystal structure shows channels containing ethanol guests which are hydrogen-bonded to carboxylate oxygens of the framework. The pyridyl rings of the framework alternate between 'open' and 'closed' positions along the channels resulting in large variation in the channel cross-sectional area from ca. 1.4 by 2.3 A at the narrowest point to 4.9 by 5.3 A at the widest. Despite the very small windows, the ethanol guests (of van der Waals diameter ca. 4.2-6.1 A) may be reversibly desorbed and sorbed into the structure quantitatively, as shown by in situ variable-temperture IR spectroscopy and XRPD. The single-crystal structure of the desolvated form [Co(INA)(2)] shows that there is no change in the overall connectivity on desolvation, but the rotational positions of the pyridine rings are altered. This suggests that pyridyl rotation may occur to allow guests to pass in and out. When the synthesis was conducted in 1-propanol solvent [Co(INA)(2)]x0.5Pr(n)OHxH(2)O, was obtained, and a single-crystal X-ray structure revealed the same overall connectivity as in but with pyridine rings disordered over closed and open positions. There was no evidence of included guests from X-ray crystallography, suggesting that they are also highly disordered. Variable-temperature XRPD performed on bulk samples showed peaks which were unsymmetrical and exhibited shoulders, suggesting that for each pattern obtained the material actually consisted of several closely-related phases. The movements of the peaks during desolvation showed the presence of intermediate phases before the final desolvated product was formed. The peak positions of the intermediate phases matched more closely with the calculated pattern for than with or, suggesting that they may have disordered structures similar to. The results also suggest that the intermediate phase represents an initial increase in volume before a larger decrease in volume occurs to give the final desolvated material.

Entities:  

Year:  2004        PMID: 15381984     DOI: 10.1039/B404485A

Source DB:  PubMed          Journal:  Dalton Trans        ISSN: 1477-9226            Impact factor:   4.390


  4 in total

Review 1.  Chemistry and application of flexible porous coordination polymers.

Authors:  Sareeya Bureekaew; Satoru Shimomura; Susumu Kitagawa
Journal:  Sci Technol Adv Mater       Date:  2008-04-25       Impact factor: 8.090

2.  catena-Poly[[bis-(μ(2)-4-amino-benzene-sulfonato-κO:O)disilver]-bis-(μ(2)-4,4'-bipyridine-κN:N')].

Authors:  Guang-Chuan Ou; Min Zhang; Xian-You Yuan; Yong-Qiang Dai
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-11-22

Review 3.  Metal-organic frameworks and self-assembled supramolecular coordination complexes: comparing and contrasting the design, synthesis, and functionality of metal-organic materials.

Authors:  Timothy R Cook; Yao-Rong Zheng; Peter J Stang
Journal:  Chem Rev       Date:  2012-11-02       Impact factor: 60.622

Review 4.  Flexible two-dimensional square-grid coordination polymers: structures and functions.

Authors:  Hiroshi Kajiro; Atsushi Kondo; Katsumi Kaneko; Hirofumi Kanoh
Journal:  Int J Mol Sci       Date:  2010-09-30       Impact factor: 5.923

  4 in total

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