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Relevant bibliographies by topics / Supramolecular MS

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Journal articles

Academic literature on the topic 'Supramolecular MS'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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Journal articles on the topic "Supramolecular MS"

1

Yang, Jiajia, Mohan Bhadbhade, William A. Donald, et al. "Self-assembled supramolecular cages containing ruthenium(ii) polypyridyl complexes." Chemical Communications 51, no. 21 (2015): 4465–68. http://dx.doi.org/10.1039/c4cc10292d.

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Substitution-inert, redox- and photo-active ruthenium(ii) complexes based on 2,2′,6′,2′′-terpyridine ligands were self-assembled into discrete supramolecular cages via coordination to palladium(ii) centres and characterised by NMR, ESI-MS and X-ray crystallography.

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2

Yilmaz, Erkan, and Mustafa Soylak. "Supramolecular solvent microextraction of gold prior to its determination by microsample injection system coupled with flame atomic absorption spectrometry." RSC Adv. 4, no. 88 (2014): 47396–401. http://dx.doi.org/10.1039/c4ra08209e.

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A supramolecular solvent based liquid–liquid microextraction (SsLLME) system for gold was developed prior to its determination by a microsample injection system coupled with flame atomic absorption spectrometric (MS-FAAS).

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3

Aydin, Funda, Erkan Yilmaz, and Mustafa Soylak. "Supramolecular solvent-based microextraction method for cobalt traces in food samples with optimization Plackett–Burman and central composite experimental design." RSC Advances 5, no. 115 (2015): 94879–86. http://dx.doi.org/10.1039/c5ra15856g.

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A new microextraction method based on formation of supramolecular solvent (Ss) was developed by using of chemometric optimization method for cobalt determination with microsampling flame atomic absorption spectrometry (MS-FAAS).

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4

Al Isawi, Wisam A., and Gellert Mezei. "Doubling the Carbonate-Binding Capacity of Nanojars by the Formation of Expanded Nanojars." Molecules 26, no. 11 (2021): 3083. http://dx.doi.org/10.3390/molecules26113083.

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Anion binding and extraction from solutions is currently a dynamic research topic in the field of supramolecular chemistry. A particularly challenging task is the extraction of anions with large hydration energies, such as the carbonate ion. Carbonate-binding complexes are also receiving increased interest due to their relevance to atmospheric CO2 fixation. Nanojars are a class of self-assembled, supramolecular coordination complexes that have been shown to bind highly hydrophilic anions and to extract even the most hydrophilic ones, including carbonate, from water into aliphatic solvents. Here we present an expanded nanojar that is able to bind two carbonate ions, thus doubling the previously reported carbonate-binding capacity of nanojars. The new nanojar is characterized by detailed single-crystal X-ray crystallographic studies in the solid state and electrospray ionization mass spectrometric (including tandem MS/MS) studies in solution.

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5

Bill, Nathan L., Masatoshi Ishida, Yuki Kawashima, et al. "Long-lived charge-separated states produced in supramolecular complexes between anionic and cationic porphyrins." Chem. Sci. 5, no. 10 (2014): 3888–96. http://dx.doi.org/10.1039/c4sc00803k.

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6

Ebbert, Kristina E., Laura Schneider, André Platzek, et al. "Resolution of minor size differences in a family of heteroleptic coordination cages by trapped ion mobility ESI-MS." Dalton Transactions 48, no. 29 (2019): 11070–75. http://dx.doi.org/10.1039/c9dt01814j.

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Trapped ion mobility mass spectrometry shows its power as analytical tool in supramolecular chemistry by discriminating ten heteroleptic coordination cage derivatives, only differing slightly in size.

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7

Bravin, Carlo, Elena Badetti, Rakesh Puttreddy, et al. "Binding Profiles of Self-Assembled Supramolecular Cages from ESI-MS Based Methodology." Chemistry - A European Journal 24, no. 12 (2018): 2936–43. http://dx.doi.org/10.1002/chem.201704725.

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8

Matmin, Juan, Leny Yuliati, Mustaffa Shamsuddin, and Hendrik Oktendy Lintang. "Supramolecular Hydrogen Bonding Interactions of Novel 1,3,5-Benzenetricarbonyl Trisubstituted Alkyl for Anion Sensor Applications." Advanced Materials Research 925 (April 2014): 228–32. http://dx.doi.org/10.4028/www.scientific.net/amr.925.228.

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Herein we report the first example of benzene-1,3,5-tricarboxamide bearing hydrophobic aminododecane side chains (1) which spontaneously forms supramolecular network by a hydrogen bonding interaction. The compound 1 was synthesized by Schotten-Baumann reaction of 1,3,5-benzenetricarbonyl trichloride and 1-aminododecane in the presence of N,N-diisopropylethylamine. Nuclear Magnetic Resonance (NMR), Mass Spectrometry (MS), and Fourier Transform Infrared (FTIR) spectroscopies have proved the successful synthesis of 1 in 93% as white powder solid. The supramolecular organization was successfully utilized for sensing of nitrate anions by deformation of the hydrogen bonding to form inactive nitroso groups.

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9

Mathieson, Jennifer S., Mali H. Rosnes, Victor Sans, Philip J. Kitson, and Leroy Cronin. "Continuous parallel ESI-MS analysis of reactions carried out in a bespoke 3D printed device." Beilstein Journal of Nanotechnology 4 (April 29, 2013): 285–91. http://dx.doi.org/10.3762/bjnano.4.31.

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Herein, we present an approach for the rapid, straightforward and economical preparation of a tailored reactor device using three-dimensional (3D) printing, which can be directly linked to a high-resolution electrospray ionisation mass spectrometer (ESI-MS) for real-time, in-line observations. To highlight the potential of the setup, supramolecular coordination chemistry was carried out in the device, with the product of the reactions being recorded continuously and in parallel by ESI-MS. Utilising in-house-programmed computer control, the reactant flow rates and order were carefully controlled and varied, with the changes in the pump inlets being mirrored by the recorded ESI-MS spectra.

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10

Peuravuori, J., P. Bursáková, and K. Pihlaja. "ESI-MS analyses of lake dissolved organic matter in light of supramolecular assembly." Analytical and Bioanalytical Chemistry 389, no. 5 (2007): 1559–68. http://dx.doi.org/10.1007/s00216-007-1553-z.

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