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Guest-Induced Assembly of Tetracarboxyl-Cavitand and Tetra(3-pyridyl)-Cavitand into a Heterodimeric Capsule via Hydrogen Bonds and CH—Halogen and/or CH—π Interaction: Control of the Orientation of the Encapsulated Guest.

Authors :
Kobayashi, Kenji
Ishii, Kei
Sakamoto, Shigeru
Shirasaka, Toshiaki
Yamaguchi, Kentaro
Source :
Journal of the American Chemical Society. 9/3/2003, Vol. 125 Issue 35, p10615-10624. 10p. 17 Diagrams, 3 Charts, 23 Graphs.
Publication Year :
2003

Abstract

The guest- or solvent-induced assembly of a tetracarboxyl-cavitand 1 and a tetra(3-pyridyl)cavitand 2 into a heterodimeric capsule 1·2 in a rim-to-rim fashion via four intermolecular CO[sub 2]H···N hydrogen bonds has been investigated both in solution and in the solid state. In the ¹H NMR study, a 1:1 mixture of 1a and 2a (R = (CH[sub 2])[sub 6]CH[sub 3]) in CDCI[sub 3] gave a mixture of various complicated aggregates, whereas this mixture in CDCI[sub 2]CDCI[sub 2] or p-xylene-d[sub 10] exclusively produced the heterodimeric capsule 1a·2a. It was found that an appropriate 1,4-disubstituted-benzene is a suitable guest for inducing the exclusive formation of 1a·2a in CDCI[sub 3]. The ability of a guest to induce the formation of guest-encapsulating heterodimeric capsule, guest@(1a·2a), increased in the order p-ethyltoluene < 1-ethyl-4-methoxybenzene ≤1-ethyl-4-iodobenzene ≤ 1,4-dibromobenzene < 1-iodo-4-methoxybenzene ≤ 1,4-dimethoxybenzene ≤ 1,4-diiodobenzene. The ¹H NMR study revealed that a CH-halogen interaction between the inner protons of the methylene-bridge rims (-O-H[sub out]CH[sub in]-O-) of the 1a and 2a units and the halogen atoms of 1,4-dihalobenzenes and a CH-π interaction between the methoxy protons of 1,4-dimethoxybenzene and the aromatic cavities of the la and 2a units play important roles in the formation of 1,4-dihalobenzene @ (1a·2a) and 1,4-dimethoxybenzene@(1a·2a), respectively. A preliminary single-crystal X-ray diffraction analysis of guest@ (1b·2b) (R = (CH[sub 2])[sub 2]Ph; guest = 1-iodo-4-methoxybenzene or p-xylene) confirmed that the guest encapsulated in 1b·2b is oriented with the long axis of the guest along the long axis of 1b·2b and that the iodo and the methoxy groups of the encapsulated 1-iodo-4-methoxybenzene are specifically oriented with respect to the cavities of the 2b and 1b units, respectively. [ABSTRACT FROM AUTHOR]

Subjects

Subjects :
*CHEMISTRY

Details

Language :
English
ISSN :
00027863
Volume :
125
Issue :
35
Database :
Academic Search Index
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
10819436
Full Text :
https://doi.org/10.1021/ja035337q