## Abstract We report the synthesis of modified __Cram__‐type cavitands bearing one or two fluorescent labels for single‐molecule spectroscopic studies of __vasekite__ conformational switching (__Scheme 3__). Syntheses were performed by stepwise bridging of the four couples of neighboring H‐bonded
Functionalized and Partially or Differentially Bridged Resorcin[4]arene Cavitands: Synthesis and Solid-State Structures
✍ Scribed by Vladimir A. Azov; Philip J. Skinner; Yoko Yamakoshi; Paul Seiler; Volker Gramlich; François Diederich
- Book ID
- 102858039
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- German
- Weight
- 553 KB
- Volume
- 86
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
We report the synthesis and structural characterization of modified Cram‐type, resorcin[4]arene‐based cavitands. Two main loci on the cavitand backbone were selected for structural modification: the upper part (wall domain) and the lower part (legs). Synthesis of unsymmetrically bridged cavitands with different wall components (i.e., 7, 8, and 14–18) was performed by stepwise bridging of the four couples of neighboring, H‐bonded OH‐groups of octol 1a (Schemes 1, 2, 4, and 5). Cavitands with modified legs (i.e., 20, 24, 27, and 28), targeted for surface immobilization, were synthesized by short routes starting from suitable aldehyde starting materials incorporating either the fully preformed leg moieties or functional precursors to the final legs (Schemes 7–10). The new cavitand substitution patterns described in this paper should enable the construction of a wide variety of functional architectures in the future. X‐Ray crystallography afforded the characterization of cavitands 2c (Fig. 3) and 24 (Fig. 7) in the vase conformation, with 2c featuring a well‐ordered CH~2~Cl~2~ guest molecule in its cavity. A particular highlight is the X‐ray crystal‐structure determination of octanitro derivative 19 (Scheme 6), which, for the first time, shows a cavitand, lacking substituents in the ortho‐position to the two O‐atoms of the four resorcinol moieties, in the kite‐conformation (Fig. 5).
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