2001
DOI: 10.1021/ja005695i
|View full text |Cite
|
Sign up to set email alerts
|

A Double-Walled Hexagonal Supermolecule Assembled by Guest Binding

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

1
13
0
1

Year Published

2001
2001
2008
2008

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 44 publications
(15 citation statements)
references
References 16 publications
1
13
0
1
Order By: Relevance
“…3) as well as on two different weak interactions and reversible bonds. Provisionally, it should suffice to categorize these by the operating interactions: two different metal-ligand interactions, [9][10][11][12][13] metal-ligand coordination + reversible covalent bond, [14,15] metal-ligand coordination + ion-dipole interaction, [7,16] metal-ligand coordination + hydrogen bonding, [17,18] metal-ligand coordination + p-p stacking, [19] reversible covalent bond + ion-dipole interaction, [20] and two different reversible covalent bonds. [21] Supramolecular multicomponent (n !…”
mentioning
confidence: 99%
“…3) as well as on two different weak interactions and reversible bonds. Provisionally, it should suffice to categorize these by the operating interactions: two different metal-ligand interactions, [9][10][11][12][13] metal-ligand coordination + reversible covalent bond, [14,15] metal-ligand coordination + ion-dipole interaction, [7,16] metal-ligand coordination + hydrogen bonding, [17,18] metal-ligand coordination + p-p stacking, [19] reversible covalent bond + ion-dipole interaction, [20] and two different reversible covalent bonds. [21] Supramolecular multicomponent (n !…”
mentioning
confidence: 99%
“…Interest in the oligonuclear analogs is much less intense [1,2] despite the obvious advantage of a greater possibility for the formation of crystals by recrystallization that should result from these compounds with lower molecular weights. Interest in the oligonuclear analogs is much less intense [1,2] despite the obvious advantage of a greater possibility for the formation of crystals by recrystallization that should result from these compounds with lower molecular weights.…”
Section: Commentmentioning
confidence: 99%
“…The reaction of transition metals with organic linkages has led to a rich assortment of molecular geometries, including the equivalents of squares, pentagons, hexagons, cubes, tetrahedra, and double hexagons [1][2][3][4][5][6][7][8][9]. These molecules have been designed to have high structural integrity, adjustable cavities, high surface area, and uniform pores to serve as new materials for ion exchange, sensor applications, molecular or chiral recognition, catalysis, environmental remediation, and drug delivery.…”
Section: Introductionmentioning
confidence: 99%
“…The only use of silicon as the metal in a dicatechol is found in two studies by Shea and co-workers. They examined the reaction of the simplest such catechol (8) with triethoxyphenylsilane in the presence of triethylamine (to neutralize the acid produced and to provide the counterion), but obtained a linear oligomer roughly of the type 4 (but higher oligomerization) with end-group oxidation [27]. The product darkened upon standing in air.…”
mentioning
confidence: 99%