Host-guest complexation. 42. Preorganization strongly enhances the tendency of hemispherands to form hemispheraplexes

Kenneth M. Doxsee, Martin Feigel, Kent D. Stewart, James Canary, Carolyn B. Knobler, Donald J. Cram

Research output: Contribution to journalArticle

Abstract

The design and syntheses of four new macrocyclic host compounds (1-4, Chart I) are reported which contain three cyclic urea carbonyls and two anisyl-like oxygens alternately arranged to bind alkali metal or alkylammonium ion guests. The macroring systems are completed with a 1,3-xylyl bridging unit containing a methoxy in its 2- and a methyl in its 4-position (1, 2) or a 3,5-dimethylphenyl group in its 2-position (3, 4). Hosts 1-4 are rigidified further with a trimethylene bridge that spans the two aryl oxygens. Hosts 1 and 2 differ only by the absence in 1 and the presence in 2 of methyl groups in the positions para to the two aryl oxygens. Hosts 3 and 4 are diastereomers, whose interconvertibility by ring inversion is blocked by steric limitations imposed on the system by the two bridging units. The configurational identities of 3 and 4 were established from their crystal structures. Hosts 5-7 (Chart I) were also prepared. Macrocycle 5 resembles 4 except the aryl oxygen trimethylene bridge is replaced by hydrogens. In 6 and 7, the trimethylene bridge is in place, but the 1,3-xylyl bridge is replaced by hydrogens. The crystal structures of the more conformationally mobile compounds 5 and 6 show that the dipoles of the carbonyl groups are better arranged to cancel one another than those of the more rigid hosts, 3 and 4. The crystal structure of 2·(CH3)3CNH3+ is exactly what was expected from molecular model examination. Free energies and association constants were determined for 1-4 and 7 binding Li+, Na+, K+, Rb+, Cs+, NH4+, CH3NH3+, and (CH3)3CNH3+ picrates at 25°C in CDCl3 saturated with D2O. The resulting -ΔG° values ranged from 7.3 (7 binding Li+) to 16.7 kcal mol-1 (3 binding Na+). The -ΔG° values correlate with the degrees of preorganization of the hosts for binding. Cycle 2 was the strongest binding host. Diastereomer 3, the second strongest complexing host, bound the eight guests 2.25 ± 0.75 (extremes) kcal mol-1 better than diastereomer 4. The crystal structure of 3 shows its binding sites to be better organized for complexation than those of 4. Host 2, containing methyl groups para to the aryl oxygens, bound the eight guests an average of 3.7 kcal mol-1 better than 1 without the two methyl groups. This effect is attributed to greater steric inhibitions of solvation of the binding sites of 2 than of 1. Host 7, containing the trimethylene but lacking the xylyl bridge, bound the eight guests with -(ΔG°)av = 7.5 kcal mol-1, which is lower by 4.4-7.1 kcal mol-1 than the hosts containing the latter bridge. Host 3 was found to complex 1 mol of (CH3)3C-O-N=O (1H NMR). The -ΔG° value of known host 8 was used for comparisons.

Original languageEnglish (US)
Pages (from-to)3098-3107
Number of pages10
JournalJournal of the American Chemical Society
Volume109
Issue number10
StatePublished - 1987

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Complexation
Oxygen
Crystal structure
Picrates
Binding sites
Hydrogen
Macrocyclic Compounds
Binding Sites
Free Association
Alkali Metals
Molecular Models
Solvation
Alkali metals
Urea
Free energy
Ions
Nuclear magnetic resonance
Association reactions
cyclopropane

ASJC Scopus subject areas

  • Chemistry(all)

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Host-guest complexation. 42. Preorganization strongly enhances the tendency of hemispherands to form hemispheraplexes. / Doxsee, Kenneth M.; Feigel, Martin; Stewart, Kent D.; Canary, James; Knobler, Carolyn B.; Cram, Donald J.

In: Journal of the American Chemical Society, Vol. 109, No. 10, 1987, p. 3098-3107.

Research output: Contribution to journalArticle

Doxsee, Kenneth M. ; Feigel, Martin ; Stewart, Kent D. ; Canary, James ; Knobler, Carolyn B. ; Cram, Donald J. / Host-guest complexation. 42. Preorganization strongly enhances the tendency of hemispherands to form hemispheraplexes. In: Journal of the American Chemical Society. 1987 ; Vol. 109, No. 10. pp. 3098-3107.
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abstract = "The design and syntheses of four new macrocyclic host compounds (1-4, Chart I) are reported which contain three cyclic urea carbonyls and two anisyl-like oxygens alternately arranged to bind alkali metal or alkylammonium ion guests. The macroring systems are completed with a 1,3-xylyl bridging unit containing a methoxy in its 2- and a methyl in its 4-position (1, 2) or a 3,5-dimethylphenyl group in its 2-position (3, 4). Hosts 1-4 are rigidified further with a trimethylene bridge that spans the two aryl oxygens. Hosts 1 and 2 differ only by the absence in 1 and the presence in 2 of methyl groups in the positions para to the two aryl oxygens. Hosts 3 and 4 are diastereomers, whose interconvertibility by ring inversion is blocked by steric limitations imposed on the system by the two bridging units. The configurational identities of 3 and 4 were established from their crystal structures. Hosts 5-7 (Chart I) were also prepared. Macrocycle 5 resembles 4 except the aryl oxygen trimethylene bridge is replaced by hydrogens. In 6 and 7, the trimethylene bridge is in place, but the 1,3-xylyl bridge is replaced by hydrogens. The crystal structures of the more conformationally mobile compounds 5 and 6 show that the dipoles of the carbonyl groups are better arranged to cancel one another than those of the more rigid hosts, 3 and 4. The crystal structure of 2·(CH3)3CNH3+ is exactly what was expected from molecular model examination. Free energies and association constants were determined for 1-4 and 7 binding Li+, Na+, K+, Rb+, Cs+, NH4+, CH3NH3+, and (CH3)3CNH3+ picrates at 25°C in CDCl3 saturated with D2O. The resulting -ΔG° values ranged from 7.3 (7 binding Li+) to 16.7 kcal mol-1 (3 binding Na+). The -ΔG° values correlate with the degrees of preorganization of the hosts for binding. Cycle 2 was the strongest binding host. Diastereomer 3, the second strongest complexing host, bound the eight guests 2.25 ± 0.75 (extremes) kcal mol-1 better than diastereomer 4. The crystal structure of 3 shows its binding sites to be better organized for complexation than those of 4. Host 2, containing methyl groups para to the aryl oxygens, bound the eight guests an average of 3.7 kcal mol-1 better than 1 without the two methyl groups. This effect is attributed to greater steric inhibitions of solvation of the binding sites of 2 than of 1. Host 7, containing the trimethylene but lacking the xylyl bridge, bound the eight guests with -(ΔG°)av = 7.5 kcal mol-1, which is lower by 4.4-7.1 kcal mol-1 than the hosts containing the latter bridge. Host 3 was found to complex 1 mol of (CH3)3C-O-N=O (1H NMR). The -ΔG° value of known host 8 was used for comparisons.",
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TY - JOUR

T1 - Host-guest complexation. 42. Preorganization strongly enhances the tendency of hemispherands to form hemispheraplexes

AU - Doxsee, Kenneth M.

AU - Feigel, Martin

AU - Stewart, Kent D.

AU - Canary, James

AU - Knobler, Carolyn B.

AU - Cram, Donald J.

PY - 1987

Y1 - 1987

N2 - The design and syntheses of four new macrocyclic host compounds (1-4, Chart I) are reported which contain three cyclic urea carbonyls and two anisyl-like oxygens alternately arranged to bind alkali metal or alkylammonium ion guests. The macroring systems are completed with a 1,3-xylyl bridging unit containing a methoxy in its 2- and a methyl in its 4-position (1, 2) or a 3,5-dimethylphenyl group in its 2-position (3, 4). Hosts 1-4 are rigidified further with a trimethylene bridge that spans the two aryl oxygens. Hosts 1 and 2 differ only by the absence in 1 and the presence in 2 of methyl groups in the positions para to the two aryl oxygens. Hosts 3 and 4 are diastereomers, whose interconvertibility by ring inversion is blocked by steric limitations imposed on the system by the two bridging units. The configurational identities of 3 and 4 were established from their crystal structures. Hosts 5-7 (Chart I) were also prepared. Macrocycle 5 resembles 4 except the aryl oxygen trimethylene bridge is replaced by hydrogens. In 6 and 7, the trimethylene bridge is in place, but the 1,3-xylyl bridge is replaced by hydrogens. The crystal structures of the more conformationally mobile compounds 5 and 6 show that the dipoles of the carbonyl groups are better arranged to cancel one another than those of the more rigid hosts, 3 and 4. The crystal structure of 2·(CH3)3CNH3+ is exactly what was expected from molecular model examination. Free energies and association constants were determined for 1-4 and 7 binding Li+, Na+, K+, Rb+, Cs+, NH4+, CH3NH3+, and (CH3)3CNH3+ picrates at 25°C in CDCl3 saturated with D2O. The resulting -ΔG° values ranged from 7.3 (7 binding Li+) to 16.7 kcal mol-1 (3 binding Na+). The -ΔG° values correlate with the degrees of preorganization of the hosts for binding. Cycle 2 was the strongest binding host. Diastereomer 3, the second strongest complexing host, bound the eight guests 2.25 ± 0.75 (extremes) kcal mol-1 better than diastereomer 4. The crystal structure of 3 shows its binding sites to be better organized for complexation than those of 4. Host 2, containing methyl groups para to the aryl oxygens, bound the eight guests an average of 3.7 kcal mol-1 better than 1 without the two methyl groups. This effect is attributed to greater steric inhibitions of solvation of the binding sites of 2 than of 1. Host 7, containing the trimethylene but lacking the xylyl bridge, bound the eight guests with -(ΔG°)av = 7.5 kcal mol-1, which is lower by 4.4-7.1 kcal mol-1 than the hosts containing the latter bridge. Host 3 was found to complex 1 mol of (CH3)3C-O-N=O (1H NMR). The -ΔG° value of known host 8 was used for comparisons.

AB - The design and syntheses of four new macrocyclic host compounds (1-4, Chart I) are reported which contain three cyclic urea carbonyls and two anisyl-like oxygens alternately arranged to bind alkali metal or alkylammonium ion guests. The macroring systems are completed with a 1,3-xylyl bridging unit containing a methoxy in its 2- and a methyl in its 4-position (1, 2) or a 3,5-dimethylphenyl group in its 2-position (3, 4). Hosts 1-4 are rigidified further with a trimethylene bridge that spans the two aryl oxygens. Hosts 1 and 2 differ only by the absence in 1 and the presence in 2 of methyl groups in the positions para to the two aryl oxygens. Hosts 3 and 4 are diastereomers, whose interconvertibility by ring inversion is blocked by steric limitations imposed on the system by the two bridging units. The configurational identities of 3 and 4 were established from their crystal structures. Hosts 5-7 (Chart I) were also prepared. Macrocycle 5 resembles 4 except the aryl oxygen trimethylene bridge is replaced by hydrogens. In 6 and 7, the trimethylene bridge is in place, but the 1,3-xylyl bridge is replaced by hydrogens. The crystal structures of the more conformationally mobile compounds 5 and 6 show that the dipoles of the carbonyl groups are better arranged to cancel one another than those of the more rigid hosts, 3 and 4. The crystal structure of 2·(CH3)3CNH3+ is exactly what was expected from molecular model examination. Free energies and association constants were determined for 1-4 and 7 binding Li+, Na+, K+, Rb+, Cs+, NH4+, CH3NH3+, and (CH3)3CNH3+ picrates at 25°C in CDCl3 saturated with D2O. The resulting -ΔG° values ranged from 7.3 (7 binding Li+) to 16.7 kcal mol-1 (3 binding Na+). The -ΔG° values correlate with the degrees of preorganization of the hosts for binding. Cycle 2 was the strongest binding host. Diastereomer 3, the second strongest complexing host, bound the eight guests 2.25 ± 0.75 (extremes) kcal mol-1 better than diastereomer 4. The crystal structure of 3 shows its binding sites to be better organized for complexation than those of 4. Host 2, containing methyl groups para to the aryl oxygens, bound the eight guests an average of 3.7 kcal mol-1 better than 1 without the two methyl groups. This effect is attributed to greater steric inhibitions of solvation of the binding sites of 2 than of 1. Host 7, containing the trimethylene but lacking the xylyl bridge, bound the eight guests with -(ΔG°)av = 7.5 kcal mol-1, which is lower by 4.4-7.1 kcal mol-1 than the hosts containing the latter bridge. Host 3 was found to complex 1 mol of (CH3)3C-O-N=O (1H NMR). The -ΔG° value of known host 8 was used for comparisons.

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