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LETTERS
PUBLISHED ONLINE: 30 NOVEMBER 2015 | DOI: 10.1038/NMAT4508
Solvent-free, supersoft and superelastic
bottlebrush melts and networks
1 2 1
William F. M. Daniel , Joanna Burdyńska , Mohammad Vatankhah-Varnoosfaderani ,
2 1† 1 3
Krzysztof Matyjaszewski , Jarosław Paturej , Michael Rubinstein , Andrey V. Dobrynin
and Sergei S. Sheiko1*
Polymer gels are the only viable class of synthetic materials
with a Young’s modulus below 100 kPa conforming to biological
applications1–3 , yet those gel properties require a solvent
fraction4–7 . The presence of a solvent can lead to phase
separation, evaporation and leakage on deformation, dimin-
ishing gel elasticity and eliciting inflammatory responses
in any surrounding tissues. Here, we report solvent-free,
supersoft and superelastic polymer melts and networks pre-
pared from bottlebrush macromolecules. The brush-like archi-
tecture expands the diameter of the polymer chains, diluting
their entanglements without markedly increasing stiness.
This adjustable interplay between chain diameter and sti-
ness makes it possible to tailor the network’s elastic modulus
and extensibility without the complications associated with a
swollen gel. The b
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