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Carbon dioxide sorbents with propylamine groups-silica functionalized with a fractional factorial design approach.

Langmuir : the ACS journal of surfaces and colloids

Aziz B, Zhao G, Hedin N.
PMID: 21361345
Langmuir. 2011 Apr 05;27(7):3822-34. doi: 10.1021/la104629m. Epub 2011 Mar 01.

Mesoporous silica particles (Davisil) were functionalized with aminopropyltriethoxysilane (APTES) in a fractional factorial design with 19 different synthesis and uptake experiments. The number of amino groups and the uptake of CO(2) were optimized in a 2(V)(5-1) design. Most important...

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Aziz B, Zhao G, Hedin N. Carbon dioxide sorbents with propylamine groups-silica functionalized with a fractional factorial design approach. Langmuir. 2011;27(7):3822-34doi: 10.1021/la104629m.
Aziz, B., Zhao, G., & Hedin, N. (2011). Carbon dioxide sorbents with propylamine groups-silica functionalized with a fractional factorial design approach. Langmuir : the ACS journal of surfaces and colloids, 27(7), 3822-34. https://doi.org/10.1021/la104629m
Aziz, Baroz, et al. "Carbon dioxide sorbents with propylamine groups-silica functionalized with a fractional factorial design approach." Langmuir : the ACS journal of surfaces and colloids vol. 27,7 (2011): 3822-34. doi: https://doi.org/10.1021/la104629m
Aziz B, Zhao G, Hedin N. Carbon dioxide sorbents with propylamine groups-silica functionalized with a fractional factorial design approach. Langmuir. 2011 Apr 05;27(7):3822-34. doi: 10.1021/la104629m. Epub 2011 Mar 01. PMID: 21361345.
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Lewis base-promoted hydrosilylation of cyclic malonates: synthesis of beta-substituted aldehydes and gamma-substituted amines.

The Journal of organic chemistry

Frost CG, Hartley BC.
PMID: 19348489
J Org Chem. 2009 May 01;74(9):3599-602. doi: 10.1021/jo900390d.

The Lewis base-promoted hydrosilylation of cyclic malonates provides a convenient synthesis of beta-substituted aldehydes. No over-reduction to the primary alcohol is observed as the aldehyde functionality is protected until a subsequent hydrolysis step. The utility of the method is...

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Frost CG, Hartley BC. Lewis base-promoted hydrosilylation of cyclic malonates: synthesis of beta-substituted aldehydes and gamma-substituted amines. J Org Chem. 2009;74(9):3599-602doi: 10.1021/jo900390d.
Frost, C. G., & Hartley, B. C. (2009). Lewis base-promoted hydrosilylation of cyclic malonates: synthesis of beta-substituted aldehydes and gamma-substituted amines. The Journal of organic chemistry, 74(9), 3599-602. https://doi.org/10.1021/jo900390d
Frost, Christopher G, and Hartley, Benjamin C. "Lewis base-promoted hydrosilylation of cyclic malonates: synthesis of beta-substituted aldehydes and gamma-substituted amines." The Journal of organic chemistry vol. 74,9 (2009): 3599-602. doi: https://doi.org/10.1021/jo900390d
Frost CG, Hartley BC. Lewis base-promoted hydrosilylation of cyclic malonates: synthesis of beta-substituted aldehydes and gamma-substituted amines. J Org Chem. 2009 May 01;74(9):3599-602. doi: 10.1021/jo900390d. PMID: 19348489.
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Facile synthesis of optically pure 1,2-diaryl (and 1-Alkyl-2-aryl) ethyl and propylamines.

Organic letters

García Ruano JL, Alemán J, Soriano JF.
PMID: 12605488
Org Lett. 2003 Mar 06;5(5):677-80. doi: 10.1021/ol027464h.

A concise high-yielding route to synthetically useful 1,2-diaryl (and 1-alkyl-2-aryl) ethyl and propylamines in high enantiomeric purity is described. The key step of this route is the completely stereoselective addition of lithium (R)-ortho-(p-toluenesulfinyl)benzylic carbanions to (S)-N-p-toluenesulfinylimines, which takes place...

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García Ruano JL, Alemán J, Soriano JF. Facile synthesis of optically pure 1,2-diaryl (and 1-Alkyl-2-aryl) ethyl and propylamines. Org Lett. 2003;5(5):677-80doi: 10.1021/ol027464h.
García Ruano, J. L., Alemán, J., & Soriano, J. F. (2003). Facile synthesis of optically pure 1,2-diaryl (and 1-Alkyl-2-aryl) ethyl and propylamines. Organic letters, 5(5), 677-80. https://doi.org/10.1021/ol027464h
García Ruano, José L, et al. "Facile synthesis of optically pure 1,2-diaryl (and 1-Alkyl-2-aryl) ethyl and propylamines." Organic letters vol. 5,5 (2003): 677-80. doi: https://doi.org/10.1021/ol027464h
García Ruano JL, Alemán J, Soriano JF. Facile synthesis of optically pure 1,2-diaryl (and 1-Alkyl-2-aryl) ethyl and propylamines. Org Lett. 2003 Mar 06;5(5):677-80. doi: 10.1021/ol027464h. PMID: 12605488.
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Temperature-induced uptake of CO2 and formation of carbamates in mesocaged silica modified with n-propylamines.

Langmuir : the ACS journal of surfaces and colloids

Bacsik Z, Atluri R, Garcia-Bennett AE, Hedin N.
PMID: 20218553
Langmuir. 2010 Jun 15;26(12):10013-24. doi: 10.1021/la1001495.

Adsorption-mediated CO(2) separation can reduce the cost of carbon capture and storage. The reduction in cost requires adsorbents with high capacities for CO(2) sorption and high CO(2)-over-N(2) selectivity. Amine-modified sorbents are promising candidates for carbon capture. To investigate the...

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Bacsik Z, Atluri R, Garcia-Bennett AE, et al. Temperature-induced uptake of CO2 and formation of carbamates in mesocaged silica modified with n-propylamines. Langmuir. 2010;26(12):10013-24doi: 10.1021/la1001495.
Bacsik, Z., Atluri, R., Garcia-Bennett, A. E., & Hedin, N. (2010). Temperature-induced uptake of CO2 and formation of carbamates in mesocaged silica modified with n-propylamines. Langmuir : the ACS journal of surfaces and colloids, 26(12), 10013-24. https://doi.org/10.1021/la1001495
Bacsik, Zoltán, et al. "Temperature-induced uptake of CO2 and formation of carbamates in mesocaged silica modified with n-propylamines." Langmuir : the ACS journal of surfaces and colloids vol. 26,12 (2010): 10013-24. doi: https://doi.org/10.1021/la1001495
Bacsik Z, Atluri R, Garcia-Bennett AE, Hedin N. Temperature-induced uptake of CO2 and formation of carbamates in mesocaged silica modified with n-propylamines. Langmuir. 2010 Jun 15;26(12):10013-24. doi: 10.1021/la1001495. PMID: 20218553.
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Showing 1 to 4 of 4 entries