JPWO2023276873A5 - - Google Patents

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JPWO2023276873A5
JPWO2023276873A5 JP2023531896A JP2023531896A JPWO2023276873A5 JP WO2023276873 A5 JPWO2023276873 A5 JP WO2023276873A5 JP 2023531896 A JP2023531896 A JP 2023531896A JP 2023531896 A JP2023531896 A JP 2023531896A JP WO2023276873 A5 JPWO2023276873 A5 JP WO2023276873A5
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cyclic olefin
olefin polymer
structural unit
ring
bonded
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Priority claimed from PCT/JP2022/025271 external-priority patent/WO2023276873A1/en
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Claims (10)

ノルボルネン骨格を有する環状オレフィン重合体であって、
前記環状オレフィン重合体が、環状オレフィン共重合体または環状オレフィン開環重合体であり、
下記要件(a)を満たすことを特徴とする、環状オレフィン重合体。
(要件(a))
当該環状オレフィン重合体は、鎖状オレフィンである構成単位(A)とノルボルネン骨格を有する環状オレフィンを含む構成単位(B)とからなり、
13C-NMRで測定した前記構成単位(B)-前記構成単位(A)-前記構成単位(B)の連鎖におけるメソ構造とラセモ構造との存在比率(ラセモ構造/メソ構造)が0.01~100である。
A cyclic olefin polymer having a norbornene skeleton,
The cyclic olefin polymer is a cyclic olefin copolymer or a cyclic olefin ring-opening polymer,
A cyclic olefin polymer characterized by satisfying the following requirement (a).
(Requirement (a))
The cyclic olefin polymer consists of a structural unit (A) that is a chain olefin and a structural unit (B) that contains a cyclic olefin having a norbornene skeleton,
The abundance ratio of meso structure and racemo structure (racemo structure/meso structure) in the chain of the structural unit (B) - the structural unit (A) - the structural unit (B) measured by 13 C-NMR is 0.01. ~100.
請求項1に記載の環状オレフィン重合体であって、
前記環状オレフィン重合体は環状オレフィン共重合体であり、
前記環状オレフィン共重合体が、
前記構成単位(A)として、エチレンまたは炭素数3~30のα-オレフィンから導かれる構成単位を30~80mol%と、
前記構成単位(B)として、下記一般式[Z-I]、下記一般式[Z-II]、下記一般式[Z-III]および下記一般式[Z-IV]からなる群より選択される1種または2種以上の環状モノマーから導かれる構成単位を20~70mol%含み、
Figure 2023276873000001
(上記式[Z-I]中、uは0または1であり、vは0または正の整数であり、wは0または1である。R61~R78ならびにRa1およびRb1は、それぞれ独立に水素原子、ハロゲン原子、および炭化水素基からなる群より選択される1種または2種以上を含み、R75~R78は、互いに結合して単環または多環を形成していてもよく、かつ前記単環または前記多環が二重結合を有していてもよい。また、R75とR76とで、またはR77とR78とでアルキリデン基を形成していてもよい。)
Figure 2023276873000002
(上記式[Z-II]中、xおよびdは0または1以上の整数であり、yおよびzは0、1または2である。R81~R99は、それぞれ独立に水素原子、ハロゲン原子、および炭化水素基から選ばれ、R89およびR90が結合している炭素原子と、R93が結合している炭素原子またはR91が結合している炭素原子とは、直接あるいは炭素原子数1~3のアルキレン基を介して結合していてもよい。また、y=z=0のとき、R95とR92またはR95とR99とは互いに結合して単環または多環の芳香族環を形成していてもよい。)
Figure 2023276873000003
(上記式[Z-III]中、nおよびmはそれぞれ独立に0、1または2であり、qは1、2または3である。R18~R31はそれぞれ独立に、水素原子、フッ素原子を除くハロゲン原子、またはフッ素原子を除くハロゲン原子で置換されていてもよい炭素原子数1~20の炭化水素基である。)
Figure 2023276873000004
(一般式[Z-IV]中、xは0または1以上の整数であり、R111~R118は、それぞれ独立に水素原子、ハロゲン原子、および炭化水素基から選ばれる。R121~R124は、それぞれ独立に水素原子、ハロゲン原子、および炭化水素基から選ばれ、隣接する2つの基は互いに結合して単環または多環の芳香環を形成していてもよい。)
前記構成単位(A)と前記構成単位(B)との合計は100mol%である、環状オレフィン重合体。
The cyclic olefin polymer according to claim 1,
The cyclic olefin polymer is a cyclic olefin copolymer,
The cyclic olefin copolymer is
As the structural unit (A), 30 to 80 mol% of a structural unit derived from ethylene or an α-olefin having 3 to 30 carbon atoms;
The structural unit (B) is selected from the group consisting of the following general formula [Z-I], the following general formula [Z-II], the following general formula [Z-III], and the following general formula [Z-IV] Contains 20 to 70 mol% of structural units derived from one or more cyclic monomers,
Figure 2023276873000001
(In the above formula [Z-I], u is 0 or 1, v is 0 or a positive integer, and w is 0 or 1. R 61 to R 78 and R a1 and R b1 are each independently contains one or more selected from the group consisting of a hydrogen atom, a halogen atom, and a hydrocarbon group, and R 75 to R 78 may be bonded to each other to form a monocyclic or polycyclic ring; The monocyclic ring or the polycyclic ring may have a double bond. Also, R 75 and R 76 or R 77 and R 78 may form an alkylidene group. )
Figure 2023276873000002
(In the above formula [Z-II], x and d are 0 or an integer of 1 or more, and y and z are 0, 1 or 2. R 81 to R 99 each independently represent a hydrogen atom or a halogen atom. , and hydrocarbon groups, and the carbon atom to which R 89 and R 90 are bonded, and the carbon atom to which R 93 is bonded or the carbon atom to which R 91 is bonded are directly or by the number of carbon atoms. They may be bonded via 1 to 3 alkylene groups.Also, when y=z=0, R 95 and R 92 or R 95 and R 99 are bonded to each other to form a monocyclic or polycyclic aromatic (May form a family ring.)
Figure 2023276873000003
(In the above formula [Z-III], n and m are each independently 0, 1 or 2, and q is 1, 2 or 3. R 18 to R 31 are each independently a hydrogen atom, a fluorine atom A hydrocarbon group having 1 to 20 carbon atoms that may be substituted with a halogen atom excluding fluorine atoms, or a halogen atom excluding fluorine atoms.)
Figure 2023276873000004
(In the general formula [Z-IV], x is 0 or an integer of 1 or more, and R 111 to R 118 are each independently selected from a hydrogen atom, a halogen atom, and a hydrocarbon group. R 121 to R 124 are each independently selected from a hydrogen atom, a halogen atom, and a hydrocarbon group, and two adjacent groups may be bonded to each other to form a monocyclic or polycyclic aromatic ring.)
A cyclic olefin polymer in which the total of the structural unit (A) and the structural unit (B) is 100 mol%.
請求項1または2に記載の環状オレフィン重合体であって、
さらに下記要件(b)を満たすことを特徴とする、環状オレフィン重合体。
(要件(b))
13C-NMRで測定した前記構成単位(B)-前記構成単位(B)の連鎖が構成単位(B)に占める割合が0.1mol%以上20.0mol%以下である。
The cyclic olefin polymer according to claim 1 or 2,
A cyclic olefin polymer further satisfying the following requirement (b).
(Requirement (b))
The ratio of the chain of the structural unit (B) to the structural unit (B) measured by 13 C-NMR in the structural unit (B) is 0.1 mol% or more and 20.0 mol% or less.
請求項1または2に記載の環状オレフィン重合体であって、
示差走査熱量計(DSC)で測定される、前記環状オレフィン共重合体または前記環状オレフィン開環重合体のガラス転移温度が50℃以上250℃以下である、環状オレフィン重合体。
The cyclic olefin polymer according to claim 1 or 2 ,
A cyclic olefin polymer, wherein the cyclic olefin copolymer or the cyclic olefin ring-opening polymer has a glass transition temperature of 50° C. or more and 250° C. or less, as measured by a differential scanning calorimeter (DSC).
請求項1または2に記載の環状オレフィン重合体であって、
示差走査熱量計(DSC)で測定される、前記環状オレフィン共重合体または前記環状オレフィン開環重合体のガラス転移温度が50℃以上180℃以下である、環状オレフィン重合体。
The cyclic olefin polymer according to claim 1 or 2 ,
A cyclic olefin polymer, wherein the cyclic olefin copolymer or the cyclic olefin ring-opening polymer has a glass transition temperature of 50° C. or higher and 180° C. or lower, as measured by a differential scanning calorimeter (DSC).
請求項1または2に記載の環状オレフィン重合体であって、
前記環状オレフィン共重合体または前記環状オレフィン開環重合体の極限粘度が0.1[dL/g]以上5.0[dL/g]以下である、環状オレフィン重合体。
The cyclic olefin polymer according to claim 1 or 2 ,
A cyclic olefin polymer, wherein the cyclic olefin copolymer or the cyclic olefin ring-opening polymer has an intrinsic viscosity of 0.1 [dL/g] or more and 5.0 [dL/g] or less.
請求項1または2に記載の環状オレフィン重合体を含む、環状オレフィン重合体組成物。 A cyclic olefin polymer composition comprising the cyclic olefin polymer according to claim 1 or 2 . 請求項7に記載の環状オレフィン重合体組成物であって、
光学部品、フィルム包材、光学フィルム、または医療用部品に用いられる、環状オレフィン重合体組成物。
The cyclic olefin polymer composition according to claim 7,
A cyclic olefin polymer composition used for optical parts, film packaging materials, optical films, or medical parts.
請求項1または2に記載の環状オレフィン重合体を含む、成形体。 A molded article comprising the cyclic olefin polymer according to claim 1 or 2 . 請求項9に記載の成形体であって、
光学部品、フィルム包材、光学フィルム、または医療用部品である、成形体。
The molded article according to claim 9,
Molded objects that are optical parts, film packaging materials, optical films, or medical parts.
JP2023531896A 2021-06-28 2022-06-24 Pending JPWO2023276873A1 (en)

Applications Claiming Priority (3)

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JP2021106711 2021-06-28
JP2022006837 2022-01-20
PCT/JP2022/025271 WO2023276873A1 (en) 2021-06-28 2022-06-24 Cyclic olefin polymer, cyclic olefin polymer composition, and molded object

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JPWO2023276873A1 JPWO2023276873A1 (en) 2023-01-05
JPWO2023276873A5 true JPWO2023276873A5 (en) 2023-11-15

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JP3817015B2 (en) 1997-04-14 2006-08-30 三井化学株式会社 Cyclic olefin copolymer and use thereof
JP2000264925A (en) * 1999-03-15 2000-09-26 Mitsui Chemicals Inc Syndiotactic propylene-cyclic olefin copolymer and its molded product
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