Abstract
A norbornene polymer comprising a repeating unit derived from a norbornene monomer having a cyclic hydrocarbon structure (I) derived from the norbornene ring which constitutes at least a part of the main chain, another cyclic hydrocarbon structure (II), which shares one carbon-carbon bond with the cyclic hydrocarbon structure (I) and has 4 to 6 carbon atoms, and a monocyclic or polycyclic hydrocarbon structure (III), which shares one carbon-carbon bond with the cyclic hydrocarbon structure (II), in a proportion of 20 to 100 mol % based on the whole repeating unit of the polymer, wherein the number average molecular weight is within a range of 1,000 to 1,000,000, and a peak area (A) on a high magnetic field side and a peak area (B) on a low magnetic field side in methylene peaks derived from the methylene groups in the cyclic hydrocarbon structure (III) in a 13C-NMR spectrum as determined in heavy chloroform (TMS standard) satisfy a relationship of the expression:
Filing date: May 5, 2000
Issue date: Feb 25, 2003
Inventors: Naoki Tanahashi, Hidehiro Ito, Toshihide Murakami
Assignee: Nippon Zeon Co., Ltd.
Primary Examiner: Bernard Lipman
Attorney: Dinsmore & Shohl LLP
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What is claimed is:
1. A norbornene polymer comprising a repeating unit derived from a norbornene monomer having a cyclic hydrocarbon structure (I) derived from the norbornene ring which constitutes at least a part of the main chain, another cyclic hydrocarbon structure (II), which shares one carbon-carbon bond with the cyclic hydrocarbon structure (I) and has 4 to 6 carbon atoms, and a monocyclic or polycyclic hydrocarbon structure (III), which shares one carbon-carbon bond with the cyclic hydrocarbon structure (II), in a proportion of 20 to 100 mol % based on the whole repeating unit of the polymer, wherein the number average molecular weight is within a range of 1,000 to 1,000,000, and a peak area (A) on a high magnetic field side and a peak area (B) on a low magnetic field side in methylene peaks derived from the methylene groups in the cyclic hydrocarbon structure (III) in a 13C-NMR spectrum as determined in heavy chloroform (TMS standard) satisfy a relationship of the expression:
B/(AB)0.30.
2. The norbornene polymer according to claim 1, which is a hydrogenated product of a thermoplastic norbornene addition polymer.
3. The norbornene polymer according to claim 1, which is a hydrogenated product of a thermoplastic norbornene ring-opening polymer.
4. The norbornene polymer according to claim 1, wherein the cyclic hydrocarbon structure (II) has a saturated and fused alicyclic structure.
5. The norbornene polymer according to claim 1, wherein the cyclic hydrocarbon structure (III) has a saturated and fused alicyclic structure.
6. The norbornene polymer according to claim 5, wherein the saturated and fused alicyclic structure is a cyclohexane ring.
7. The norbornene polymer according to claim 1, wherein the repeating unit derived from the norbornene monomer is represented by the formula (1):
wherein
- l and m are individually 0, 1 or 2;
- n is 0, 1 or 2;
- lmn2;
- R1, R2 and R7 to R18 are independently a hydrogen atom, hydrocarbon group, halogen atom, hydroxyl group, ester group, alkoxy group, cyano group, amide group, imide group or silyl group, or a hydrocarbon group substituted by a polar group (a halogen atom, hydroxyl group, ester group, alkoxy group, cyano group, amide group, imide group or silyl group), with the proviso that:
- R14 and R15 are bonded to each other to form a monocyclic or polycyclic hydrocarbon structure when n is 0;
- any one or both of R14 and R17, and R15 and R18 are bonded to each other to form a monocyclic or polycyclic hydrocarbon structure when n is 1 or 2, provided that when both R14 and R17, and R15 and R18 are bonded to each other to form a cyclic hydrocarbon structure, the cyclic hydrocarbon structure may be a fused polycycle which shares at least one carbon-carbon bond with each other; and
- R3 to R6 are all hydrogen atoms, or R4 and R5 among them may form a single bond together, and in this case, both R3 and R6 are hydrogen atoms.
8. The norbornene polymer according to claim 7, wherein the repeating unit derived from the norbornene monomer is represented by the formula (9):
9. The norbornene polymer according to claim 1, which comprises 20 to 100 mol % of the repeating unit represented by the formula (1) derived from the norbornene monomer, and 0 to 80 mol % of a repeating unit derived from any other monomer copolymerizable with the norbornene monomer.
10. The norbornene polymer according to claim 1, which is a hydrogenated product of a ring-opening polymer of a tetrahydrofluorene selected from among 1,4-methano-1,4,4a,9a-tetrahydrofluorene and substituted derivatives thereof.
11. The norbornene polymer according to claim 1, which is a hydrogenated product of a ring-opening polymer of a octahydrofluorene selected from among 1,4-methano-1,4,4a,4b,5,8,8a,9a-octahydro-9H-fluorene and substituted derivatives thereof.
12. The norbornene polymer according to claim 1, which is a hydrogenated product of a ring-opening copolymer of a tetrahydrofluorene selected from among 1,4-methano-1,4,4a,9a-tetrahydrofluorene and substituted derivatives thereof with a tetrahydrododecene selected from among tetracyclo4.4.0.12,5.17,10-3-dodecene and substituted derivatives thereof.
13. A process for producing the norbornene polymer according to claim 1, which comprises polymerizing a monomer or monomer mixture comprising 20 to 100 mol % of a norbornene monomer (i) of a fused polycyclic structure having a norbornene ring structure (IA), a cyclic hydrocarbon structure (IIA), which shares one carbon-carbon bond with the norbornene ring structure (IA) and has 4 to 6 carbon atoms, and a monocyclic or polycyclic hydrocarbon structure (IIIA), which shares one carbon-carbon bond with the cyclic hydrocarbon structure (IIA) and has at least one carbon-carbon unsaturated bond in its ring, the compositional ratio (a:b) between an endo form (a) and an exo form (b) which are stereoisomers of said norbornene monomer being within a range of 70:30 to 100:0, and 0 to 80 mol % of any other monomer (ii) copolymerizable with the norbornene monomer, and then hydrogenating the resultant polymer at a temperature of 200 C. or lower.
14. The production process according to claim 13, which comprises subjecting the monomer or monomer composition to ring-opening (co)polymerization and then saturating at least 80 mol % of the carbon-carbon double bond in the main chain and at least 50 mol % of the monocyclic or polycyclic hydrocarbon structure (IIIA) having at least one carbon-carbon unsaturated bond in the ring of the side chain by hydrogenation.
15. The production process according to claim 13, which comprises subjecting the monomer or monomer composition to addition (co)polymerization and then saturating at least 50 mol % of the monocyclic or polycyclic hydrocarbon structure (IIIA) having at least one carbon-carbon unsaturated bond in the ring of the side chain by hydrogenation.
16. The production process according to claim 13, wherein the norbornene monomer (i) is a compound represented by the formula (2):
wherein
- l and m are individually 0, 1 or 2;
- n is 0, 1 or 2;
- lmn2; and
- R1, R2 and R7 to R18 are independently a hydrogen atom, hydrocarbon group, halogen atom, hydroxyl group, ester group, alkoxy group, cyano group, amide group, imide group or silyl group, or a hydrocarbon group substituted by a polar group (a halogen atom, hydroxyl group, ester group, alkoxy group, cyano group, amide group, imide group or silyl group), with the proviso that:
- R14 and R15 are bonded to each other to form a monocyclic or polycyclic hydrocarbon structure having at least one carbon-carbon unsaturated bond in its ring when n is 0;
- any one or both of R14 and R17, and R15 and R18 are bonded to each other to form a monocyclic or polycyclic hydrocarbon structure having at least one carbon-carbon unsaturated bond in its ring when n is 1 or 2, provided that when both R14 and R17, and R15 and R18 are bonded to each other to form a cyclic hydrocarbon structure, the cyclic hydrocarbon structure may be a fused polycycle which shares at least one carbon-carbon bond with each other.
17. The production process according to claim 16, wherein the compound represented by the formula (2) is a tetrahydrofluorene selected from among 1,4-methano-1,4,4a,9a-tetrahydrofluorene represented by the formula (5):
and substituted derivatives thereof.
18. The production process according to claim 16, wherein the compound represented by the formula (2) is a tetrahydrofluorene selected from among 1,4-methano-1,4,4a,4b,5,8,8a,9a-octahydro-9H-fluorene represented by the formula (6):
and substituted derivatives thereof.
19. The production process according to claim 13, wherein said any other monomer (ii) is another norbornene monomer (iii) than the norbornene monomer (i).
20. The production process according to claim 19, wherein the norbornene monomer (iii) is a tetrahydrododecene selected from among tetracyclo-4.4.0.12,5.17,10-3-dodecene represented by the formula (10):
and substituted derivatives thereof.
21. A molding material comprising the norbornene polymer according to claim 1.
22. The molding material according to claim 21, which is a resin composition comprising the norbornene polymer and at least one compounding additive selected from the group consisting of rubbery polymers, other thermoplastic resins, stabilizers, lubricants, inorganic fine particles, ultraviolet absorbents, antistatic agents, fillers, flame retardants, flame retardant auxiliaries, pigments, dyes, anti-fogging agents, compatibilizers, slip agents, anti-blocking agents, natural oil, synthetic oil, wax, plasticizers, crosslinking agents and crosslinking.
23. The molding material according to claim 22, wherein the resin composition comprises a thermoplastic elastomer as the rubbery polymer.
24. The molding material according to claim 22, wherein the resin composition comprises an antioxidant as the stabilizer.
25. The molding material according to claim 22, wherein the resin composition comprises a lubricant.
26. The molding material according to claim 22, wherein the resin composition comprises a flame retardant.
27. The molding material according to claim 22, wherein the resin composition comprises a crosslinking agent.
28. The molding material according to claim 22, wherein the resin composition comprises an organic filler or inorganic filler as the filler.
29. A molded or formed product formed of the molding material according to claim 21.
30. The molded or formed product according to claim 29, which is a medical equipment, electrical insulating member, electronic part treating equipment or optical member.
31. The norbornene polymer according to claim 1, wherein the glass transition temperature of the norbornene polymer is at least 145 C.