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Dr STEPHEN ARGENT's Outputs (69)

Amides Do Not Always Work: Observation of Guest Binding in an Amide-Functionalized Porous Metal-Organic Framework (2016)
Journal Article
Benson, O., da Silva, I., Argent, S. P., Cabot, R., Savage, M., Godfrey, H. G., Yan, Y., Parker, S. F., Manuel, P., Lennox, M. J., Mitra, T., Easun, T. L., Lewis, W., Blake, A. J., Besley, E., Yang, S., & Schröder, M. (2016). Amides Do Not Always Work: Observation of Guest Binding in an Amide-Functionalized Porous Metal-Organic Framework. Journal of the American Chemical Society, 138(45), 14828-14831. https://doi.org/10.1021/jacs.6b08059

An amide-functionalized metal organic framework (MOF) material, MFM-136, shows a high CO2 uptake of 12.6 mmol g–1 at 20 bar and 298 K. MFM-136 is the first example of an acylamide pyrimidyl isophthalate MOF without open metal sites and, thus, provide... Read More about Amides Do Not Always Work: Observation of Guest Binding in an Amide-Functionalized Porous Metal-Organic Framework.

Amides Do Not Always Work: Observation of Guest Binding in an Amide-Functionalized Porous Metal-Organic Framework (2016)
Journal Article
Benson, O., da Silva, I., Argent, S. P., Cabot, R., Savage, M., Godfrey, H. G., Yan, Y., Parker, S. F., Manuel, P., Lennox, M. J., Mitra, T., Easun, T. L., Lewis, W., Blake, A. J., Besley, E., Yang, S., & Schröder, M. (2016). Amides Do Not Always Work: Observation of Guest Binding in an Amide-Functionalized Porous Metal-Organic Framework. Journal of the American Chemical Society, 138(45), 14828–14831. https://doi.org/10.1021/jacs.6b08059

An amide-functionalized metal organic framework (MOF) material, MFM-136, shows a high CO2 uptake of 12.6 mmol g–1 at 20 bar and 298 K. MFM-136 is the first example of an acylamide pyrimidyl isophthalate MOF without open metal sites and, thus, provide... Read More about Amides Do Not Always Work: Observation of Guest Binding in an Amide-Functionalized Porous Metal-Organic Framework.

Amides Do Not Always Work: Observation of Guest Binding in an Amide-Functionalized Porous Metal–Organic Framework (2016)
Journal Article
Benson, O., da Silva, I., Argent, S. P., Cabot, R., Savage, M., Godfrey, H. G., Yan, Y., Parker, S. F., Manuel, P., Lennox, M. J., Mitra, T., Easun, T. L., Lewis, W., Blake, A. J., Besley, E., Yang, S., & Schröder, M. (2016). Amides Do Not Always Work: Observation of Guest Binding in an Amide-Functionalized Porous Metal–Organic Framework. Journal of the American Chemical Society, 138(45), 14828-14831. https://doi.org/10.1021/jacs.6b08059

An amide-functionalised metal organic frame-work (MOF) material, MFM-136, shows a high CO2 uptake of 12.6 mmol g-1 at 20 bar and 298 K. MFM-136 is the first example of acylamide pyrimidyl isophthalate MOF without open metal sites, and thus provides a... Read More about Amides Do Not Always Work: Observation of Guest Binding in an Amide-Functionalized Porous Metal–Organic Framework.

Selective Adsorption of Sulfur Dioxide in a Robust Metal-Organic Framework Material (2016)
Journal Article
Savage, M., Cheng, Y., Easun, T. L., Eyley, J. E., Argent, S. P., Warren, M. R., Lewis, W., Murray, C., Tang, C. C., Frogley, M. D., Cinque, G., Sun, J., Rudić, S., Murden, R. T., Benham, M. J., Fitch, A. N., Blake, A. J., Ramirez-Cuesta, A. J., Yang, S., & Schröder, M. (2016). Selective Adsorption of Sulfur Dioxide in a Robust Metal-Organic Framework Material. Advanced Materials, 28(39), 8705-8711. https://doi.org/10.1002/adma.201602338

Selective adsorption of SO2 is realized in a porous metal–organic framework material, and in-depth structural and spectroscopic investigations using X-rays, infrared, and neutrons define the underlying interactions that cause SO2 to bind more strongl... Read More about Selective Adsorption of Sulfur Dioxide in a Robust Metal-Organic Framework Material.

Proton Conduction in a Phosphonate-Based Metal–Organic Framework Mediated by Intrinsic “Free Diffusion inside a Sphere” (2016)
Journal Article
Pili, S., Argent, S. P., Morris, C. G., Rought, P., García-Sakai, V., Silverwood, I. P., Easun, T. L., Li, M., Warren, M. R., Murray, C. A., Tang, C. C., Yang, S., & Schröder, M. (2016). Proton Conduction in a Phosphonate-Based Metal–Organic Framework Mediated by Intrinsic “Free Diffusion inside a Sphere”. Journal of the American Chemical Society, 138(20), 6352-6355. https://doi.org/10.1021/jacs.6b02194

Assembly of high nuclearity clusters from a family of tripodal tris-carboxylate ligands (2016)
Journal Article
Argent, S. P., Tarassova, I., Greenaway, A., Nowell, H., Barnett, S. A., Warren, M. R., Tang, C. C., Morris, C. G., Lewis, W., Champness, N. R., Schröder, M., & Blake, A. J. (2016). Assembly of high nuclearity clusters from a family of tripodal tris-carboxylate ligands. Polyhedron, 120, 18-29. https://doi.org/10.1016/j.poly.2016.04.029

A family of four tris-carboxylic acid ligands 1,3,5-tris(4′-carboxybiphenyl-2-yl)benzene (H3L1), 1,3,5-tris-2-carboxyphenylbenzene (H3L2), 1,3,5-tris(4″-carboxy-para-terphenyl-2-yl)benzene (H3L3) and 1,3,5-tris(3′-carboxybiphenyl-2-yl)benzene (H3L4)... Read More about Assembly of high nuclearity clusters from a family of tripodal tris-carboxylate ligands.

Thymine functionalised porphyrins, synthesis and heteromolecular surface-based self-assembly (2014)
Journal Article
Slater, A. G., Hu, Y., Yang, L., Argent, S. P., Lewis, W., Blunt, M. O., & Champness, N. R. (in press). Thymine functionalised porphyrins, synthesis and heteromolecular surface-based self-assembly. RSC Advances, 6, https://doi.org/10.1039/C4SC03531C

The synthesis and surface-based self-assembly of thymine-functionalised porphyrins is described. Reaction of 1-formylphenyl-3-benzoyl-thymine with suitable pyrollic species leads to the formation of tetra-(phenylthymine)porphyrin (tetra-TP) or mono-t... Read More about Thymine functionalised porphyrins, synthesis and heteromolecular surface-based self-assembly.

Bis-thioether-substituted perylene diimides: Structural, electrochemical, and spectroelectrochemical properties (2013)
Journal Article
Slater, A. G., Davies, E. S., Argent, S. P., Lewis, W., Blake, A. J., McMaster, J., & Champness, N. R. (2013). Bis-thioether-substituted perylene diimides: Structural, electrochemical, and spectroelectrochemical properties. Journal of Organic Chemistry, 78(7), 2853-2862. https://doi.org/10.1021/jo400026r

The synthesis and separation of the 1,6- and 1,7- isomers of N,N′-bis(alkyl)diadamantylthio-3,4,9,10-perylenetetracarboxylic acid diimide are reported. Investigations of the structural, electrochemical, spectroscopic, and spectroelectrochemical prope... Read More about Bis-thioether-substituted perylene diimides: Structural, electrochemical, and spectroelectrochemical properties.

Bis-morpholine-substituted perylene bisimides: Impact of isomeric arrangement on electrochemical and spectroelectrochemical properties (2008)
Journal Article
Goretzki, G., Davies, E. S., Argent, S. P., Alsindi, W. Z., Blake, A. J., Warren, J. E., McMaster, J., & Champness, N. R. (2008). Bis-morpholine-substituted perylene bisimides: Impact of isomeric arrangement on electrochemical and spectroelectrochemical properties. Journal of Organic Chemistry, 73(22), 8808-8814. https://doi.org/10.1021/jo801557e

(Graph Presented) The synthesis and separation of the 1,6- and 1,7- isomers of N,N′-bis(n-butyl)dimorpholino-3,4:9,10-perylenetetracarboxylic acid bisimide are reported. Investigations of the electrochemical and spectroscopic, in particular, spectroe... Read More about Bis-morpholine-substituted perylene bisimides: Impact of isomeric arrangement on electrochemical and spectroelectrochemical properties.