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Merck

254185

Sigma-Aldrich

Copper(I) bromide

99.999% trace metals basis

Sinónimos:

Cuprous bromide

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About This Item

Fórmula lineal:
CuBr
Número de CAS:
Peso molecular:
143.45
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23

Quality Level

assay

99.999% trace metals basis

form

powder

reaction suitability

reagent type: catalyst
core: copper

impurities

≤15.0 ppm Trace Metal Analysis

mp

504 °C (lit.)

density

4.71 g/mL at 25 °C (lit.)

application(s)

battery manufacturing

SMILES string

[Cu]Br

InChI

1S/BrH.Cu/h1H;/q;+1/p-1

InChI key

NKNDPYCGAZPOFS-UHFFFAOYSA-M

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General description

Copper(I) bromide is a faint green inorganic diamagnetic solid that has a polymeric structure like zinc sulfide. It is insoluble in water and widely used in the field of catalysis, nanomaterial synthesis, and solar cells.

Application

Copper(I) bromide can be used:
  • As a solution-processable hole transport layer (HTL) for organic solar cells (OSCs). CuBr enhances the power conversion efficiency of solar cells.
  • As a precursor to synthesize photoluminescent metal organic frameworks(MOFs).
  • To synthesize highly emissive three-coordinate copper(I) complexes as a dopant in OLEDs with maximum external quantum efficiency of 21.3%.
  • As a catalyst with ligands for atom transfer radical polymerization (ATRP) reaction of tertiary alkyl halides in 14 different solvents to determine the rate constant.
  • To synthesize macrocyclic polymer via intramolecular radical trap-assisted atom transfer radical coupling.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Denissova I and Barriault L et al.
Handbook of Reagents for Organic Synthesis null
Carla Sardo et al.
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The cyclic brush polymers, due to the unique topological structure, have shown in the previous studies higher delivery efficacy than the bottlebrush analogues as carriers for drug and gene transfer. However, to the best of knowledge, the preparation of reduction-sensitive

Artículos

We carry a large variety of electrophiles and nucleophiles that are widely used in C–C bond-forming reactions. This group of products contains many organometallic reagents as well as commonly-used alkylating and acylating reagents.

We presents an article about a micro review of reversible addition/fragmentation chain transfer (RAFT) polymerization. RAFT (Reversible Addition/Fragmentation Chain Transfer) polymerization is a reversible deactivation radical polymerization (RDRP) and one of the more versatile methods for providing living characteristics to radical polymerization.

We presents an article about Copper(I)-mediated Living Radical Polymerization in the Presence of Pyridylmethanimine Ligands, and the emergence of living radical polymerization mediated by transition metal catalysts in 1995, which was a seminal piece of work in the field of synthetic polymer chemistry.

Applying ARGET ATRP to the Growth of Polymer Brush Thin Films by Surface-initiated Polymerization

Protocolos

Sigma-Aldrich presents an article about RAFT, or Reversible Addition/Fragmentation Chain Transfer, which is a form of living radical polymerization.

We presents an article featuring procedures that describe polymerization of methyl methacrylate and vinyl acetate homopolymers and a block copolymer as performed by researchers at CSIRO.

Sigma-Aldrich presents an article about the typical procedures for polymerizing via ATRP, which demonstrates that in the following two procedures describe two ATRP polymerization reactions as performed by Prof. Dave Hadddleton′s research group at the University of Warwick.

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