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Bio-synthetic Polymer Conjugates pp 151–190Cite as

Synthesis of Terpene-Based Polymers

Part of the Advances in Polymer Science book series (POLYMER,volume 253)

Abstract

Terpenes or terpenoids are a large class of diverse biological compounds derived from isoprene. Due to their abundance in nature and desirable properties, there has been great interest in producing polymers with terpenes as either functional entities or as the main constituent. Terpene-based polymers have found applications as biomedical or liquid crystalline materials and, more importantly, have greatly contributed to the concept of sustainable polymer chemistry. The design and preparation of terpene-based polymers have involved different chemical strategies and a wide variety of polymerization techniques, making use of the chemical functionalities in terpene molecules, e.g. (conjugated) double bonds, hydroxyl and carboxyl groups. This review describes the synthetic methodologies for terpene-based polymers, classified by the position of terpene entities in the polymer chains, i.e., main chain, terminal or central group, and pendant group.

Keywords

  • Bioconjugate
  • Biohybrid
  • Polymerization
  • Synthesis
  • Terpene

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Abbreviations

Ac:

Acetyl

ADMET:

Acyclic diene metathesis

AIBN:

α,α′-Azobisisobutyronitrile

ATRP:

Atom transfer radical polymerization

BPO:

Benzoyl peroxide

Bui :

Isobutyl

Bz:

Benzyl

CDI:

1,1-Carbonyldiimidazole

Chol:

Cholesterol or cholesteryl

CholCl:

Cholesteryl chloroformate

Cy:

Cyclohexyl

DCC:

Dicyclohexylcarbodiimide

DMAP:

4-(N,N-Dimethylamino)pyridine

DMF:

N,N-Dimethylformamide

DMSO:

Dimethylsulfoxide

Et:

Ethyl

LC:

Liquid crystal/crystalline

mCPBA:

m-Chloroperbenzoic acid

Me:

Methyl

Men:

Menthol

MMA:

Methyl methacrylate

M n :

Number-average molecular weight

MW:

Molecular weight

NHS:

N-Hydroxysuccinimide

Oct:

Octoate

PCL:

Poly(ε-caprolactone)

PDI:

Polydispersity index

PEG:

Poly(ethylene glycol)

PEO:

Poly(ethylene oxide)

Ph:

Phenyl

PLA:

Poly(lactic acid)

PNIPAM:

Poly(N-isopropylacrylamide)

Pr:

Propyl

pTSA:

p-Toluenesulfonic acid

Py:

Pyridine

RAFT:

Reversible addition-fragmentation chain transfer

ROMP:

Ring-opening metathesis polymerization

ROP:

Ring-opening polymerization

TBD:

1,5,7-Triazabicyclo[4.4.0]dec-5-ene

T g :

Glass transition temperature

THF:

Tetrahydrofuran

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Acknowledgements

Financial support by the Max Planck Society (MPG) and Firmenich International SA is acknowledged.

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  1. Colloid Department, Max Planck Institute of Colloids and Interfaces, Research Campus Golm, 14424, Potsdam, Germany

    Junpeng Zhao & Helmut Schlaad

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  1. Junpeng Zhao
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  2. Helmut Schlaad
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Correspondence to Helmut Schlaad .

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  1. Research Campus Golm, Department of Colloid Chemistry, Max Planck Institute of Colloids and Int, Research Campus Golm, Potsdam, 14424, Germany

    Helmut Schlaad

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Zhao, J., Schlaad, H. (2011). Synthesis of Terpene-Based Polymers. In: Schlaad, H. (eds) Bio-synthetic Polymer Conjugates. Advances in Polymer Science, vol 253. Springer, Berlin, Heidelberg. https://doi.org/10.1007/12_2012_166

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