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Merck
CN

566098

TEMPO, polymer-bound

100-200 mesh, extent of labeling: 1.0 mmol/g loading, 1 % cross-linked with divinylbenzene

Synonym(s):

(2,2,6,6-Tetramethyl-1-piperidinyloxy, free radical), polymer-bound, PS-TEMPO

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About This Item

UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22
MDL number:
Form:
solid
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form

solid

crosslinking

1 % cross-linked with divinylbenzene

reaction suitability

reaction type: solution phase peptide synthesis, reactivity: alcohol reactive

extent of labeling

1.0 mmol/g loading

particle size

100-200 mesh

General description

TEMPO, polymer-bound (PS-TEMPO) has been synthesized via nitroxide catalyzed radical polymerization of styrene. TEMPO end-capped polystyrene (PS-TEMPO) copolymers have been synthesized for the modification of multi-walled carbon nanotubes (MWNTs). Synthesis of PS-TEMPO from polystyrene, benzoyl peroxide and TEMPO has been reported. Grafting of TEMPO onto polystyrene has been proposed via copper(I)-catalyzed azide-alkyne cycloaddition reaction.

Features and Benefits

Free radical catalyst.


Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Articles

TEMPO(2,2,6,6-四甲基哌啶氧基或2,2,6,6-四甲基哌啶1-氧基)及其衍生物在有机氧化反应催化剂中可以作为稳定的硝酰基使用。TEMPO由Lebedev和Kazarnovskii于1960年发现,其具有的稳定自由基性质得益于其庞大的取代基团阻碍了自由基与其他分子之间发生反应。


Mechanism and kinetics of nitroxide-controlled free radical polymerization. Thermal decomposition of 2, 2, 6, 6-tetramethyl-1-polystyroxypiperidines.
Ohno K, et al.
Macromolecules, 30(8), 2503-2506 (1997)
Grafting of alkoxyamine end-capped (co) polymers onto multi-walled carbon nanotubes.
Lou X, et al.
Polymer, 45(18), 6097-6102 (2004)
J. Hodges
Journal of Combinatorial Chemistry, 2, 88-88 (2000)



Global Trade Item Number

SKUGTIN
566098-5G04061833356159
566098-1G04061826697009