A polycationic dendrimer as noncovalent support for anionic organometallic complexes

R. van de Coevering; M. Kuil; R.J.M. Klein Gebbink; G. van Koten

doi:10.1039/B201491B

A polycationic dendrimer as noncovalent support for anionic organometallic complexes

R. van de Coevering
, M. Kuil
, R.J.M. Klein Gebbink
, G. van Koten

extern

Research output: Contribution to journal › Article › Academic › peer-review

Abstract

Polycationic dendrimer 1 forms a well-defined, stoichiometric assembly with eight anionic metal complexes; this assembly is successfully applied as a Lewis acidic catalyst which performs comparably to the unsupported metal complex.

Original language	English
Pages (from-to)	1636-1637
Number of pages	2
Journal	Chemical Communications
Volume	2002
Issue number	15
DOIs	https://doi.org/10.1039/B201491B
Publication status	Published - 2002

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title = "A polycationic dendrimer as noncovalent support for anionic organometallic complexes",

abstract = "Polycationic dendrimer 1 forms a well-defined, stoichiometric assembly with eight anionic metal complexes; this assembly is successfully applied as a Lewis acidic catalyst which performs comparably to the unsupported metal complex.",

author = "\{van de Coevering\}, R. and M. Kuil and \{Klein Gebbink\}, R.J.M. and \{van Koten\}, G.",

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doi = "10.1039/B201491B",

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AU - van Koten, G.

PY - 2002

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N2 - Polycationic dendrimer 1 forms a well-defined, stoichiometric assembly with eight anionic metal complexes; this assembly is successfully applied as a Lewis acidic catalyst which performs comparably to the unsupported metal complex.

AB - Polycationic dendrimer 1 forms a well-defined, stoichiometric assembly with eight anionic metal complexes; this assembly is successfully applied as a Lewis acidic catalyst which performs comparably to the unsupported metal complex.

U2 - 10.1039/B201491B

DO - 10.1039/B201491B

M3 - Article

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VL - 2002

SP - 1636

EP - 1637

JO - Chemical Communications

JF - Chemical Communications

IS - 15

ER -

A polycationic dendrimer as noncovalent support for anionic organometallic complexes

Abstract

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