Evaluation of hydrogen bonding ability of liquids and solids by C-13 NMR. Silica gel as a strong hydrogen bond donor
Abstract The chemical shift difference between signals of C(β) and C(α) of unsaturated ketones, Δδ, which we used before to measure acid strengths, has now been used to evaluate the hydrogen bond donor ability of solvents which are not acidic enough to hydronate the indicator. For such solvents ther...
Ausführliche Beschreibung
Autor*in: |
Farcaşiu, Dan [verfasserIn] |
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Format: |
Artikel |
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Sprache: |
Englisch |
Erschienen: |
1995 |
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Schlagwörter: |
hydrogen bonding, measurement by NMR NMR, hydrogen bonding evaluation by solids, hydrogen bonding ability of |
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Systematik: |
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Anmerkung: |
© J.C. Baltzer AG, Science Publishers 1995 |
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Übergeordnetes Werk: |
Enthalten in: Catalysis letters - Baltzer Science Publishers, Baarn/Kluwer Academic Publishers, 1988, 31(1995), 4 vom: Dez., Seite 351-358 |
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Übergeordnetes Werk: |
volume:31 ; year:1995 ; number:4 ; month:12 ; pages:351-358 |
Links: |
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DOI / URN: |
10.1007/BF00808599 |
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10.1007/BF00808599 doi (DE-627)OLC204013333X (DE-He213)BF00808599-p DE-627 ger DE-627 rakwb eng 540 660 VZ VA 2890 VZ rvk Farcaşiu, Dan verfasserin aut Evaluation of hydrogen bonding ability of liquids and solids by C-13 NMR. Silica gel as a strong hydrogen bond donor 1995 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © J.C. Baltzer AG, Science Publishers 1995 Abstract The chemical shift difference between signals of C(β) and C(α) of unsaturated ketones, Δδ, which we used before to measure acid strengths, has now been used to evaluate the hydrogen bond donor ability of solvents which are not acidic enough to hydronate the indicator. For such solvents there is no general correlation between H-bond donor ability and acid strength: hexa-fluoroisopropanol is a much weaker acid than acetic acid, but it is a stronger H-bond donor. The method can be applied to evaluate the H-bonding properties of solid surfaces, and it was thus found that silica gel has a much stronger H-bond donor ability than methanol or acetic acid. hydrogen bonding, measurement by NMR NMR, hydrogen bonding evaluation by solids, hydrogen bonding ability of solvents, hydrogen bonding ability of supports, hydrogen bonding ability of Ghenciu, Anca aut Enthalten in Catalysis letters Baltzer Science Publishers, Baarn/Kluwer Academic Publishers, 1988 31(1995), 4 vom: Dez., Seite 351-358 (DE-627)130436550 (DE-600)644234-1 (DE-576)025720724 1011-372X nnns volume:31 year:1995 number:4 month:12 pages:351-358 https://doi.org/10.1007/BF00808599 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_21 GBV_ILN_65 GBV_ILN_70 GBV_ILN_2006 GBV_ILN_2016 GBV_ILN_4012 GBV_ILN_4305 GBV_ILN_4314 VA 2890 AR 31 1995 4 12 351-358 |
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10.1007/BF00808599 doi (DE-627)OLC204013333X (DE-He213)BF00808599-p DE-627 ger DE-627 rakwb eng 540 660 VZ VA 2890 VZ rvk Farcaşiu, Dan verfasserin aut Evaluation of hydrogen bonding ability of liquids and solids by C-13 NMR. Silica gel as a strong hydrogen bond donor 1995 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © J.C. Baltzer AG, Science Publishers 1995 Abstract The chemical shift difference between signals of C(β) and C(α) of unsaturated ketones, Δδ, which we used before to measure acid strengths, has now been used to evaluate the hydrogen bond donor ability of solvents which are not acidic enough to hydronate the indicator. For such solvents there is no general correlation between H-bond donor ability and acid strength: hexa-fluoroisopropanol is a much weaker acid than acetic acid, but it is a stronger H-bond donor. The method can be applied to evaluate the H-bonding properties of solid surfaces, and it was thus found that silica gel has a much stronger H-bond donor ability than methanol or acetic acid. hydrogen bonding, measurement by NMR NMR, hydrogen bonding evaluation by solids, hydrogen bonding ability of solvents, hydrogen bonding ability of supports, hydrogen bonding ability of Ghenciu, Anca aut Enthalten in Catalysis letters Baltzer Science Publishers, Baarn/Kluwer Academic Publishers, 1988 31(1995), 4 vom: Dez., Seite 351-358 (DE-627)130436550 (DE-600)644234-1 (DE-576)025720724 1011-372X nnns volume:31 year:1995 number:4 month:12 pages:351-358 https://doi.org/10.1007/BF00808599 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_21 GBV_ILN_65 GBV_ILN_70 GBV_ILN_2006 GBV_ILN_2016 GBV_ILN_4012 GBV_ILN_4305 GBV_ILN_4314 VA 2890 AR 31 1995 4 12 351-358 |
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10.1007/BF00808599 doi (DE-627)OLC204013333X (DE-He213)BF00808599-p DE-627 ger DE-627 rakwb eng 540 660 VZ VA 2890 VZ rvk Farcaşiu, Dan verfasserin aut Evaluation of hydrogen bonding ability of liquids and solids by C-13 NMR. Silica gel as a strong hydrogen bond donor 1995 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © J.C. Baltzer AG, Science Publishers 1995 Abstract The chemical shift difference between signals of C(β) and C(α) of unsaturated ketones, Δδ, which we used before to measure acid strengths, has now been used to evaluate the hydrogen bond donor ability of solvents which are not acidic enough to hydronate the indicator. For such solvents there is no general correlation between H-bond donor ability and acid strength: hexa-fluoroisopropanol is a much weaker acid than acetic acid, but it is a stronger H-bond donor. The method can be applied to evaluate the H-bonding properties of solid surfaces, and it was thus found that silica gel has a much stronger H-bond donor ability than methanol or acetic acid. hydrogen bonding, measurement by NMR NMR, hydrogen bonding evaluation by solids, hydrogen bonding ability of solvents, hydrogen bonding ability of supports, hydrogen bonding ability of Ghenciu, Anca aut Enthalten in Catalysis letters Baltzer Science Publishers, Baarn/Kluwer Academic Publishers, 1988 31(1995), 4 vom: Dez., Seite 351-358 (DE-627)130436550 (DE-600)644234-1 (DE-576)025720724 1011-372X nnns volume:31 year:1995 number:4 month:12 pages:351-358 https://doi.org/10.1007/BF00808599 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_21 GBV_ILN_65 GBV_ILN_70 GBV_ILN_2006 GBV_ILN_2016 GBV_ILN_4012 GBV_ILN_4305 GBV_ILN_4314 VA 2890 AR 31 1995 4 12 351-358 |
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10.1007/BF00808599 doi (DE-627)OLC204013333X (DE-He213)BF00808599-p DE-627 ger DE-627 rakwb eng 540 660 VZ VA 2890 VZ rvk Farcaşiu, Dan verfasserin aut Evaluation of hydrogen bonding ability of liquids and solids by C-13 NMR. Silica gel as a strong hydrogen bond donor 1995 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © J.C. Baltzer AG, Science Publishers 1995 Abstract The chemical shift difference between signals of C(β) and C(α) of unsaturated ketones, Δδ, which we used before to measure acid strengths, has now been used to evaluate the hydrogen bond donor ability of solvents which are not acidic enough to hydronate the indicator. For such solvents there is no general correlation between H-bond donor ability and acid strength: hexa-fluoroisopropanol is a much weaker acid than acetic acid, but it is a stronger H-bond donor. The method can be applied to evaluate the H-bonding properties of solid surfaces, and it was thus found that silica gel has a much stronger H-bond donor ability than methanol or acetic acid. hydrogen bonding, measurement by NMR NMR, hydrogen bonding evaluation by solids, hydrogen bonding ability of solvents, hydrogen bonding ability of supports, hydrogen bonding ability of Ghenciu, Anca aut Enthalten in Catalysis letters Baltzer Science Publishers, Baarn/Kluwer Academic Publishers, 1988 31(1995), 4 vom: Dez., Seite 351-358 (DE-627)130436550 (DE-600)644234-1 (DE-576)025720724 1011-372X nnns volume:31 year:1995 number:4 month:12 pages:351-358 https://doi.org/10.1007/BF00808599 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_21 GBV_ILN_65 GBV_ILN_70 GBV_ILN_2006 GBV_ILN_2016 GBV_ILN_4012 GBV_ILN_4305 GBV_ILN_4314 VA 2890 AR 31 1995 4 12 351-358 |
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10.1007/BF00808599 doi (DE-627)OLC204013333X (DE-He213)BF00808599-p DE-627 ger DE-627 rakwb eng 540 660 VZ VA 2890 VZ rvk Farcaşiu, Dan verfasserin aut Evaluation of hydrogen bonding ability of liquids and solids by C-13 NMR. Silica gel as a strong hydrogen bond donor 1995 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © J.C. Baltzer AG, Science Publishers 1995 Abstract The chemical shift difference between signals of C(β) and C(α) of unsaturated ketones, Δδ, which we used before to measure acid strengths, has now been used to evaluate the hydrogen bond donor ability of solvents which are not acidic enough to hydronate the indicator. For such solvents there is no general correlation between H-bond donor ability and acid strength: hexa-fluoroisopropanol is a much weaker acid than acetic acid, but it is a stronger H-bond donor. The method can be applied to evaluate the H-bonding properties of solid surfaces, and it was thus found that silica gel has a much stronger H-bond donor ability than methanol or acetic acid. hydrogen bonding, measurement by NMR NMR, hydrogen bonding evaluation by solids, hydrogen bonding ability of solvents, hydrogen bonding ability of supports, hydrogen bonding ability of Ghenciu, Anca aut Enthalten in Catalysis letters Baltzer Science Publishers, Baarn/Kluwer Academic Publishers, 1988 31(1995), 4 vom: Dez., Seite 351-358 (DE-627)130436550 (DE-600)644234-1 (DE-576)025720724 1011-372X nnns volume:31 year:1995 number:4 month:12 pages:351-358 https://doi.org/10.1007/BF00808599 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_21 GBV_ILN_65 GBV_ILN_70 GBV_ILN_2006 GBV_ILN_2016 GBV_ILN_4012 GBV_ILN_4305 GBV_ILN_4314 VA 2890 AR 31 1995 4 12 351-358 |
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Evaluation of hydrogen bonding ability of liquids and solids by C-13 NMR. Silica gel as a strong hydrogen bond donor |
abstract |
Abstract The chemical shift difference between signals of C(β) and C(α) of unsaturated ketones, Δδ, which we used before to measure acid strengths, has now been used to evaluate the hydrogen bond donor ability of solvents which are not acidic enough to hydronate the indicator. For such solvents there is no general correlation between H-bond donor ability and acid strength: hexa-fluoroisopropanol is a much weaker acid than acetic acid, but it is a stronger H-bond donor. The method can be applied to evaluate the H-bonding properties of solid surfaces, and it was thus found that silica gel has a much stronger H-bond donor ability than methanol or acetic acid. © J.C. Baltzer AG, Science Publishers 1995 |
abstractGer |
Abstract The chemical shift difference between signals of C(β) and C(α) of unsaturated ketones, Δδ, which we used before to measure acid strengths, has now been used to evaluate the hydrogen bond donor ability of solvents which are not acidic enough to hydronate the indicator. For such solvents there is no general correlation between H-bond donor ability and acid strength: hexa-fluoroisopropanol is a much weaker acid than acetic acid, but it is a stronger H-bond donor. The method can be applied to evaluate the H-bonding properties of solid surfaces, and it was thus found that silica gel has a much stronger H-bond donor ability than methanol or acetic acid. © J.C. Baltzer AG, Science Publishers 1995 |
abstract_unstemmed |
Abstract The chemical shift difference between signals of C(β) and C(α) of unsaturated ketones, Δδ, which we used before to measure acid strengths, has now been used to evaluate the hydrogen bond donor ability of solvents which are not acidic enough to hydronate the indicator. For such solvents there is no general correlation between H-bond donor ability and acid strength: hexa-fluoroisopropanol is a much weaker acid than acetic acid, but it is a stronger H-bond donor. The method can be applied to evaluate the H-bonding properties of solid surfaces, and it was thus found that silica gel has a much stronger H-bond donor ability than methanol or acetic acid. © J.C. Baltzer AG, Science Publishers 1995 |
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container_issue |
4 |
title_short |
Evaluation of hydrogen bonding ability of liquids and solids by C-13 NMR. Silica gel as a strong hydrogen bond donor |
url |
https://doi.org/10.1007/BF00808599 |
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