Cavitand zn(II)-porphyrin capsules with high affinities for pyridines and N-methylimidazole.

نویسندگان

  • O Middel
  • W Verboom
  • D N Reinhoudt
چکیده

Covalent cavitand Zn(II)-porphyrins 17-20 were prepared via multistep syntheses. These host molecules show moderate to excellent binding affinities to N-methylimidazole and pyridine guests. The complexing behavior strongly depends on the spacer's length, number, and rigidity, in addition to the guest size. Cavitand capping and strapping of porphyrins strongly influence the complex formation and result in a 10-700-fold enhancement of the binding strength compared to tetraphenyl Zn(II)-porphyrin.

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Nanorings with copper(ii) and zinc(ii) centers: forcing copper porphyrins to bind axial ligands in heterometallated oligomers† †Electronic supplementary information (ESI) available: Synthesis and characterization of new compounds, UV-vis-NIR titrations and binding data for reference compounds and for the formation of linear oligomer complexes, error analysis and calculation of statistical factors. See DOI: 10.1039/c6sc01809b Click here for additional data file.

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عنوان ژورنال:
  • The Journal of organic chemistry

دوره 66 11  شماره 

صفحات  -

تاریخ انتشار 2001