Loading ...

Fast insight into nanotechnology

Access easily searchable nanoscience data, synthesis methods and literature

alkynyl-functionalized surface-cross-linked micelles

Based on

1 Articles
2016 Most recent source

Composition

1

poly ((12-[(2-methylprop-2-enoyl)oxy]dodecyl)tris(prop-2-yn-1-yl)azanium bromide/(12-[(2-methylprop-2-enoyl)oxy]dodecyl)tris(prop-2-yn-1-yl)azanium bromide/(4-vinylphenyl)boronic acid/(4-vinylphenyl)boronic acid/1,4-diazidobutane-2,3-diol/1,4-diazidobutane-2,3-diol)

Type Polymer
Formula
Role core
2

4-nitrophenyl α-D-mannopyranoside

Type Single Compound
Formula C12H15NO8
Role fillers
3

1,4-phenylene vinylene

1,4-phenylenevinylene para-divinylbenzene 1,4-divinylbenzene p-divinylbenzene divinyl benzene divinylbenzene DVB
Type Single Compound
Formula C10H10
Role loaded material

Properties

Applications

Characterization

Method Nanomaterial Variant Source
dynamic light scattering

More information/entries available to subscribers only.

Or, view sample content

Biological effects

Preparation

Method 1

Type: Chemical synthesis
Source:
Starting materials
  • (4-vinylphenyl)boronic acid
  1. aVvSaIO
  2. BsUNis
Product

alkynyl-functionalized surface-cross-linked micelles

Hydrodynamic diameter: 4.18 nm

Medium: water

Support: none

References

Full content is available to subscribers only

To view content please choose from the following:

We use cookies to improve your experience with our site. More information

Sign up for a free trial