Hydrophobicity/hydrophilicity tunable hyperbranched polystyrenes as novel supports for transition-metal nanoparticlesElectronic supplementary information (ESI) available. See DOI: 10.1039/c2cc35390c
Development of a new preparative procedure for hyperbranched polystyrene having Cl end groups (HPS-Cl) enables to prepare HPS-NR 3 + Cl − , for which the hydrophobicity/hydrophilicity is tunable by the R groups. The resulting ammonium salts behave as a good support of platinum nanoparticles, which i...
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creator | Kojima, Keisuke Chikama, Katsumi Ishikawa, Makoto Tanaka, Akihiro Nishikata, Takashi Tsutsumi, Hironori Igawa, Kazunobu Nagashima, Hideo |
description | Development of a new preparative procedure for hyperbranched polystyrene having Cl end groups (HPS-Cl) enables to prepare HPS-NR
3
+
Cl
−
, for which the hydrophobicity/hydrophilicity is tunable by the R groups. The resulting ammonium salts behave as a good support of platinum nanoparticles, which is useful for catalytic biphasic hydrogenation of alkenes.
A new preparative procedure for hyperbranched polystyrene having Cl end groups enables the preparation of HPS-NR
3
+
Cl
−
, which behaves as a good support for Pt NPs for biphasic hydrogenation of alkenes. |
doi_str_mv | 10.1039/c2cc35390c |
format | Article |
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3
+
Cl
−
, for which the hydrophobicity/hydrophilicity is tunable by the R groups. The resulting ammonium salts behave as a good support of platinum nanoparticles, which is useful for catalytic biphasic hydrogenation of alkenes.
A new preparative procedure for hyperbranched polystyrene having Cl end groups enables the preparation of HPS-NR
3
+
Cl
−
, which behaves as a good support for Pt NPs for biphasic hydrogenation of alkenes.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/c2cc35390c</identifier><language>eng</language><creationdate>2012-10</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Kojima, Keisuke</creatorcontrib><creatorcontrib>Chikama, Katsumi</creatorcontrib><creatorcontrib>Ishikawa, Makoto</creatorcontrib><creatorcontrib>Tanaka, Akihiro</creatorcontrib><creatorcontrib>Nishikata, Takashi</creatorcontrib><creatorcontrib>Tsutsumi, Hironori</creatorcontrib><creatorcontrib>Igawa, Kazunobu</creatorcontrib><creatorcontrib>Nagashima, Hideo</creatorcontrib><title>Hydrophobicity/hydrophilicity tunable hyperbranched polystyrenes as novel supports for transition-metal nanoparticlesElectronic supplementary information (ESI) available. See DOI: 10.1039/c2cc35390c</title><description>Development of a new preparative procedure for hyperbranched polystyrene having Cl end groups (HPS-Cl) enables to prepare HPS-NR
3
+
Cl
−
, for which the hydrophobicity/hydrophilicity is tunable by the R groups. The resulting ammonium salts behave as a good support of platinum nanoparticles, which is useful for catalytic biphasic hydrogenation of alkenes.
A new preparative procedure for hyperbranched polystyrene having Cl end groups enables the preparation of HPS-NR
3
+
Cl
−
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3
+
Cl
−
, for which the hydrophobicity/hydrophilicity is tunable by the R groups. The resulting ammonium salts behave as a good support of platinum nanoparticles, which is useful for catalytic biphasic hydrogenation of alkenes.
A new preparative procedure for hyperbranched polystyrene having Cl end groups enables the preparation of HPS-NR
3
+
Cl
−
, which behaves as a good support for Pt NPs for biphasic hydrogenation of alkenes.</abstract><doi>10.1039/c2cc35390c</doi><tpages>3</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | Hydrophobicity/hydrophilicity tunable hyperbranched polystyrenes as novel supports for transition-metal nanoparticlesElectronic supplementary information (ESI) available. See DOI: 10.1039/c2cc35390c |
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