Ring-opening polymerization

In polymer chemistry, ring-opening polymerization (ROP) is a form of chain-growth polymerization, in which the terminus of a polymer chain attacks cyclic monomers to form a longer polymer (see figure). The reactive center can be radical, anionic or cationic. Some cyclic monomers such as norbornene or cyclooctadiene can be polymerized to high molecular weight polymers by using metal catalysts. ROP is a versatile method for the synthesis of biopolymers.

IUPAC definition for ring-opening polymerization

A polymerization in which a cyclic monomer yields a monomeric unit which is acyclic or contains fewer cycles than the monomer.

Note: If monomer is polycyclic, the opening of a single ring is sufficient to classify the reaction as ring-opening polymerization.

Modified from the earlier definition[1]

.[2]

Penczek S.; Moad, G. Pure Appl. Chem., 2008, 80(10), 2163-2193

General scheme ionic propagation. Propagating center can be radical, cationic or anionic.

Ring-opening of cyclic monomers is often driven by the relief of bond-angle strain. Thus, as is the case for other types of polymerization, the enthalpy change in ring-opening is negative.[3]

Monomers

Cyclic monomers that are amenable to ROP include epoxides, cyclic trisiloxanes, some lactones, lactides, cyclic carbonates, and amino acid N-carboxyanhydrides.[4][5][6][7] Many strained cycloalkenes, e.g norbornene, are suitable monomers via ring-opening metathesis polymerization.

History

Ring-opening polymerization has been used since the beginning of the 1900s to produce polymers. Synthesis of polypeptides which has the oldest history of ROP, dates back to the work in 1906 by Leuchs.[8] Subsequently, the ROP of anhydro sugars provided polysaccharides, including synthetic dextran, xanthan gum, welan gum, gellan gum, diutan gum, and pullulan. Mechanisms and thermodynamics of ring-opening polymerization were established in the 1950s.[9][10] The first high-molecular weight polymers (M_n up to 10⁵) with a repeating unit were prepared by ROP as early as in 1976.[11][12]

An industrial application is the production of nylon-6.

Mechanisms

Ring-opening polymerization can proceed via radical, anionic, or cationic polymerization as described below.[13] Additionally, radical ROP is useful in producing polymers with functional groups incorporated in the backbone chain that cannot otherwise be synthesized via conventional chain-growth polymerization of vinyl monomers. For instance, radical ROP can produce polymers with ethers, esters, amides, and carbonates as functional groups along the main chain.[13][14]

Anionic ring-opening polymerization (AROP)

The general mechanism for anionic ring-opening polymerization. Polarized functional group is represented by X-Y, where the atom X (usually a carbon atom) becomes electron deficient due to the highly electron-withdrawing nature of Y (usually an oxygen, nitrogen, sulfur, etc.). The nucleophile will attack atom X, thus releasing Y-. The newly formed nucleophile will then attack the atom X in another monomer molecule, and the sequence would repeat until the polymer is formed.[14]

Anionic ring-opening polymerizations (AROP) are involve nucleophilic reagents as initiators. Monomers with a three-member ring structure - such as epoxides, aziridines, and episulfides - undergo anionic ROP.[14]

A typical example of anionic ROP is that of ε-caprolactone, initiated by an alkoxide.[14]

Cationic ring-opening polymerization

Cationic initiators and intermediates characterize cationic ring-opening polymerization (CROP). Examples of cyclic monomers that polymerize through this mechanism include lactones, lactams, amines, and ethers.[15] CROP proceeds through an S_N1 or S_N2 propagation, chain-growth process.[13] The mechanism is affected by the stability of the resulting cationic species. For example, if the atom bearing the positive charge is stabilized by electron-donating groups, polymerization will proceed by the S_N1 mechanism.[14] The cationic species is a heteroatom and the chain grows by the addition of cyclic monomers thereby opening the ring system.

Synthesis of Spandex.[16]

The monomers can be activated by Bronsted acids, carbenium ions, onium ions, and metal cations.[13]

CROP can be a living polymerization and can be terminated by nucleophilic reagents such as phenoxy anions, phosphines, or polyanions.[13] When the amount of monomers becomes depleted, termination can occur intra or intermolecularly. The active end can "backbite" the chain, forming a macrocycle. Alkyl chain transfer is also possible, where the active end is quenched by transferring an alkyl chain to another polymer.

Ring-opening metathesis polymerization

Ring-opening metathesis polymerization (ROMP) produces unsaturated polymers from cycloalkenes or bicycloalkenes. It requires organometallic catalysts.[13]

The mechanism for ROMP follows similar pathways as olefin metathesis. The initiation process involves the coordination of the cycloalkene monomer to the metal alkylidene complex, followed by a [2+2] type cycloaddition to form the metallacyclobutane intermediate that cycloreverts to form a new alkylidene species.[17][18]

General scheme of the mechanism for ROMP.

Commercially relevant unsaturated polymers synthesized by ROMP include Norsorex (polynorbornene), Vestenamer (polycyclooctene), and Metton (polycyclopentadiene).[19][20]

Thermodynamics

The formal thermodynamic criterion of a given monomer polymerizability is related to a sign of the free enthalpy (Gibbs free energy) of polymerization:

${\displaystyle \Delta G_{p}(xy)=\Delta H_{p}(xy)-T\Delta S_{p}(xy)}$

where x and y indicate monomer and polymer states, respectively (x and/or y = l (liquid), g (gaseous), c (amorphous solid), c’ (crystalline solid), s (solution)), ΔH_p(xy) and ΔSp(xy) are the corresponding enthalpy (SI unit: joule per kelvin) and entropy (SI unit: joule) of polymerization, and T is the absolute temperature (SI unit: kelvin). The free enthalpy of polymerization (ΔG_p) may be expressed as a sum of standard enthalpy of polymerization (ΔG_p°) and a term related to instantaneous monomer molecules and growing macromolecules concentrations:

${\displaystyle \Delta G_{p}=\Delta G_{p}^{\circ }+RT\ln {\frac {[...-(m)_{i+1}m^{\ast }]}{[M][...-(m)_{i}m^{\ast }]}}}$

where R is the gas constant, M is the monomer, (m)_i is the monomer in an initial state, and m^* is the active monomer. Following Flory–Huggins solution theory that the reactivity of an active center, located at a macromolecule of a sufficiently long macromolecular chain, does not depend on its degree of polymerization (DPi), and taking in to account that ΔG_p° = ΔH_p° - TΔS_p° (where ΔH_p° and ΔS_p° indicate a standard polymerization enthalpy and entropy, respectively), we obtain:

${\displaystyle \Delta G_{p}=\Delta H_{p}^{\circ }-T(\Delta S_{p}^{\circ }+R\ln[M])}$

At equilibrium (ΔG_p = 0), when polymerization is complete the monomer concentration ([M]_eq) assumes a value determined by standard polymerization parameters (ΔH_p° and ΔS_p°) and polymerization temperature:

${\displaystyle [M]_{eq}=e^{{\frac {\Delta H_{p}^{\circ }}{RT}}-{\frac {\Delta S_{p}^{\circ }}{R}}}}$

${\displaystyle \ln {\frac {DP_{n}}{DP_{n}-1}}[M]_{eq}={\frac {\Delta H_{p}^{\circ }}{RT}}-{\frac {\Delta S_{p}^{\circ }}{R}}}$

${\displaystyle [M]_{eq}={\frac {DP_{n}-1}{DP_{n}}}e^{{\frac {\Delta H_{p}^{\circ }}{RT}}-{\frac {\Delta S_{p}^{\circ }}{R}}}}$

Polymerzation is possible only when [M]₀ > [M]_eq. Eventually, at or above the so-called ceiling temperature (T_c), at which [M]_eq = [M]₀, formation of the high polymer does not occur.

${\displaystyle T_{c}={\frac {\Delta H_{p}^{\circ }}{\Delta S_{p}^{\circ }+R\ln[M]_{0}}};(\Delta H_{p}^{\circ }<0,\Delta S_{p}^{\circ }<0)}$

${\displaystyle T_{f}={\frac {\Delta H_{p}^{\circ }}{\Delta S_{p}^{\circ }+R\ln[M]_{0}}};(\Delta H_{p}^{\circ }>0,\Delta S_{p}^{\circ }>0)}$

For example, tetrahydrofuran (THF) cannot be polymerized above T_c = 84 °C, nor cyclo-octasulfur (S₈) below T_f = 159 °C.[21][22][23][24] However, for many monomers, T_c and T_f, for polymerization in the bulk, are well above or below the operable polymerization temperatures, respectively. The polymerization of a majority of monomers is accompanied by an entropy decrease, due mostly to the loss in the translational degrees of freedom. In this situation, polymerization is thermodynamically allowed only when the enthalpic contribution into ΔG_p prevails (thus, when ΔH_p° < 0 and ΔS_p° < 0, the inequality |ΔH_p| > -TΔS_p is required). Therefore, the higher the ring strain, the lower the resulting monomer concentration at equilibrium.

See also

• Ring opening metathesis polymerization
• Olefin Metathesis Polymerization

Additional reading

• Luck, edited by Rajender K. Sadhir, Russell M. (1992). Expanding Monomers: Synthesis, Characterization, and Applications. Boca Raton, Florida: CRC Press. ISBN 9780849351563.CS1 maint: extra text: authors list (link)
• Sugiyama, J; R. Nagahata; M. Goyal; M. Asai; M. Ueda; K. Takeuchi (1998). ACS Polymer Preprints. 1. 40: 90. Missing or empty |title= (help)</ref>
• Nikos Hadjichristidis, Hermis Iatrou, Marinos Pitsikalis, Georgios Sakellariou (2009). "Synthesis of Well-Defined Polypeptide-Based Materials via the Ring-Opening Polymerization of α-Amino Acid N-Carboxyanhydrides". Chemical Reviews. 109 (11): 5528–5578. doi:10.1021/cr900049t. PMID 19691359.CS1 maint: uses authors parameter (link)
• Nahrain E. Kamber, Wonhee Jeong, Robert M. Waymouth, Russell C. Pratt, Bas G. G. Lohmeijer, James L. Hedrick (2007). "Organocatalytic Ring-Opening Polymerization". Chemical Reviews. 107 (12): 5813–5840. doi:10.1021/cr068415b. PMID 17988157.CS1 maint: uses authors parameter (link)</ref>
• Matsumura, Shuichi; Tsukada, Keisuke; Toshima, Kazunobu (May 1997). "Enzyme-Catalyzed Ring-Opening Polymerization of 1,3-Dioxan-2-one to Poly(trimethylene carbonate)". Macromolecules. 30 (10): 3122–3124. Bibcode:1997MaMol..30.3122M. doi:10.1021/ma961862g.

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