17
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Modes of tetra(4-pyridyl)porphyrinatomanganese(III) ion intercalation inside natural clays

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          Metalloporphyrin ions, with planar shape, have been known to intercalate horizontally and diagonally between montmorillonite layers. Perpendicular intercalation inside montmorillonite has not been reported earlier. This work aims at achieving perpendicular intercalation inside montmorillonite in natural clays. Possible intercalation inside other forms of natural clay will also be investigated.

          Methods

          Natural clays were purified and characterized. The naked clay powder was then refluxed with tetra(4-pyridyl)porphyrinatomanganese(III) ion (MnTPyP +) solution in methanol with continuous stirring for different times. Electronic absorption spectra, atomic absorption spectra, Fourier Transform infrared spectra, scanning electron microscopy and X-ray diffraction were all used in clay characterization and in intercalation study.

          Results

          The natural clay involved different phases, namely montmorillonite, biotite, kaolinite, illite and traces of quartz. Montmorillonite clay allowed horizontal, diagonal and perpendicular intercalation of the metalloporphyrin ions. Biotite allowed only horizontal intercalation. The mode of intercalation was deduced by monitoring the clay inter-planar distance value change. Intercalation occurred inside both micro- and nano-size clay powders to different extents. The nano-powder (average size ~50 nm) showed uptake values up to 3.8 mg MnTPyP/g solid, whereas the micro-size powder (average size ~316 nm) exhibited lower uptake (2.4 mg MnTPyP/g solid). Non-expandable clay phases did not allow any intercalation. The intercalated MnTPyP + ions showed promising future supported catalyst applications.

          Conclusions

          Depending on their phase, natural clays hosted metalloporphyrin ions. Montmorillonite can allow all three possible intercalation geometries, horizontal, diagonal and for the first time perpendicular. Biotite allows horizontal intercalation only. Non-expandable clays allow no intercalation.

          Graphical abstract

          Metalloporphyrin complexes can be intercalated into montmorillonite in horizontal, perpendicular and diagonal geometries

          Electronic supplementary material

          The online version of this article (doi:10.1186/s13065-016-0153-4) contains supplementary material, which is available to authorized users.

          Related collections

          Most cited references42

          • Record: found
          • Abstract: not found
          • Article: not found

          The swelling of montmorillonite

          K Norrish (1954)
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Recent advances and actual challenges in late transition metal catalyzed hydrosilylation of olefins from an industrial point of view

              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Zeolite-encapsulated and clay-intercalated metal porphyrin, phthalocyanine and Schiff-base complexes as models for biomimetic oxidation catalysts: an overview

                Bookmark

                Author and article information

                Contributors
                ahedzyoud@najah.edu
                waheedjj@najah.edu
                waseemmansuor@yahoo.com
                mmkhan@ksu.edu.sa
                hshilal@najah.edu
                Journal
                Chem Cent J
                Chem Cent J
                Chemistry Central Journal
                Springer International Publishing (Cham )
                1752-153X
                10 March 2016
                10 March 2016
                2016
                : 10
                : 12
                Affiliations
                [ ]SSERL, Department of Chemistry, An-Najah National University, Nablus, West Bank Palestine
                [ ]King Abdullah Institute for Nanotechnology, King Saud University, P.O. Box 2454, Riyadh, 114 51 Saudi Arabia
                Article
                153
                10.1186/s13065-016-0153-4
                4787189
                26973710
                6d724726-2158-4948-9b46-e2da5c249b59
                © Zyoud et al. 2016

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 19 August 2015
                : 2 February 2016
                Funding
                Funded by: Union of Arab Universities
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2016

                Chemistry
                Chemistry

                Comments

                Comment on this article