JP6228622B2 - 強靱化アリールシクロブテンポリマー - Google Patents
強靱化アリールシクロブテンポリマー Download PDFInfo
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- JP6228622B2 JP6228622B2 JP2016056889A JP2016056889A JP6228622B2 JP 6228622 B2 JP6228622 B2 JP 6228622B2 JP 2016056889 A JP2016056889 A JP 2016056889A JP 2016056889 A JP2016056889 A JP 2016056889A JP 6228622 B2 JP6228622 B2 JP 6228622B2
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Description
K1c=f(a/W)σfa0 0.5
破壊エネルギー(G1c)を、K1c及び比率(E)から、次の式:G1c=K1c 2/Eに従って計算し、材料の比率を、Berkovichチップを備えたFisherscope HM2000 XYp圧子を使用して、ナノインデンテーションによって測定した。
Claims (8)
- 組成物であって、a)1つ以上のアリールシクロブテンモノマー、重合単位として1つ以上のアリールシクロブテンモノマーを含む1つ以上のポリマー、及びそれらの混合物から選択される硬化性材料と、b)式:R 1 −(O−A) × (OCH 2 CH 2 ) y −OR 2 を有し、式中、AがCH 2 CHRまたはCHRCH 2 であり、RがC 2〜8 ヒドロカルビル部分であり、R 1 及びR 2 が独立して、H、C 1〜20 アルキル、C 6〜20 アリール、C 7〜40 置換アリール、C 2〜20 アルケニル、C 2〜20 アルキニル、マレイミド、マレアミド/エステル、マレアミド/カルボン酸、及び(メタ)アクリロイルから選択され、xが2〜500の整数であり、yが0〜500の整数であり、R 1 及びR 2 のうちの少なくとも一方がHである、1つ以上の強靱化剤と、c)1つ以上の有機溶媒と、を含み、前記1つ以上の強靱化剤が重合単位として−(OCH2CH(CH3))−を含まず、前記組成物が剥離添加剤を含まない、前記組成物。
- R1及びR2のうちの一方がHである、請求項1に記載の前記組成物。
- 前記1つ以上の強靱化剤が、前記1つ以上の硬化性材料の合計重量に基づき、0.1〜35重量%の量で存在する、請求項1に記載の前記組成物。
- RがC2〜6ヒドロカルビル部分である、請求項1に記載の前記組成物。
- 組成物であって、重合単位として1つ以上のアリールシクロブテンモノマーを含む1つ以上の硬化性ポリマーと、式:R 1 −(O−A) × (OCH 2 CH 2 ) y −OR 2 を有し、式中、AがCH 2 CHRまたはCHRCH 2 であり、RがC 2〜8 ヒドロカルビル部分であり、R 1 及びR 2 が独立して、H、C 1〜20 アルキル、C 6〜20 アリール、C 7〜40 置換アリール、C 2〜20 アルケニル、C 2〜20 アルキニル、マレイミド、マレアミド/エステル、マレアミド/カルボン酸、及び(メタ)アクリロイルから選択され、xが2〜500の整数であり、yが0〜500の整数であり、R 1 及びR 2 のうちの少なくとも一方がHである、1つ以上の強靱化剤と、1つ以上の有機溶媒と、を含み、前記1つ以上の強靱化剤が重合単位として−(OCH2CH(CH3))−を含まず、前記組成物が剥離添加剤を含まない、組成物の層を、基材上にコーティングすることと、前記1つ以上の有機溶媒を少なくとも部分的に除去することと、前記1つ以上の硬化性ポリマーを硬化して、硬化ポリマーコーティングを形成することと、を含む、方法。
- ポリマーコーティングであって、a)重合単位として1つ以上のアリールシクロブテンモノマーを含むポリマーと、b)式:R 1 −(O−A) × (OCH 2 CH 2 ) y −OR 2 を有し、式中、AがCH 2 CHRまたはCHRCH 2 であり、RがC 2〜8 ヒドロカルビル部分であり、R 1 及びR 2 が独立して、H、C 1〜20 アルキル、C 6〜20 アリール、C 7〜40 置換アリール、C 2〜20 アルケニル、C 2〜20 アルキニル、マレイミド、マレアミド/エステル、マレアミド/カルボン酸、及び(メタ)アクリロイルから選択され、xが2〜500の整数であり、yが0〜500の整数であり、R 1 及びR 2 のうちの少なくとも一方がHである、1つ以上の強靱化剤と、を含み、前記1つ以上の強靱化剤が重合単位として−(OCH2CH(CH3))−を含まず、前記ポリマーコーティングが剥離添加剤を含まない、前記ポリマーコーティング。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14/684,187 | 2015-04-10 | ||
US14/684,187 US9296915B1 (en) | 2015-04-10 | 2015-04-10 | Toughened arylcyclobutene polymers |
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US9296915B1 (en) * | 2015-04-10 | 2016-03-29 | Dow Global Technologies Llc | Toughened arylcyclobutene polymers |
US10513568B2 (en) * | 2017-12-01 | 2019-12-24 | Rohm and Haas Electronic Materials | Methods of making stable and thermally polymerizable vinyl, amino or oligomeric phenoxy benzocyclobutene monomers with improved curing kinetics |
US20220002474A1 (en) * | 2020-07-02 | 2022-01-06 | Rohm And Haas Electronic Materials Llc | Bisbenzocyclobutene formulations |
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US4812588A (en) | 1987-12-14 | 1989-03-14 | The Dow Chemical Company | Polyorganosiloxane-bridged bisbenzocyclobutene monomers |
US5025080A (en) | 1990-03-30 | 1991-06-18 | Shell Oil Company | Resin composition from di(arylcyclobutenealkyl) ether of di(hydroxyphenyl) oligomer |
US5198527A (en) | 1990-12-24 | 1993-03-30 | The Dow Chemical Company | Arylcyclobutene terminated carbonate polymer |
US5136069A (en) | 1991-03-28 | 1992-08-04 | The Dow Chemical Company | Process for preparing vinylically-unsaturated compounds (II) |
US5138081A (en) | 1991-04-30 | 1992-08-11 | The Dow Chemical Company | Process for purifying vinylically-unsaturated organosilicon compounds |
US5854302A (en) | 1993-04-29 | 1998-12-29 | The Dow Chemical Company | Partially polymerized divinylsiloxane linked bisbenzocyclobutene resins and methods for making said resins |
JP2002530505A (ja) | 1998-11-24 | 2002-09-17 | ザ ダウ ケミカル カンパニー | 架橋性マトリックス前駆体および気孔発生体を含有する組成物、並びにそれから製造された多孔質マトリックス |
US6420093B1 (en) | 2000-02-02 | 2002-07-16 | The Dow Chemical Company | Toughened benzocyclobutene based polymers and their use in building-up printed wiring boards |
US7164197B2 (en) * | 2003-06-19 | 2007-01-16 | 3M Innovative Properties Company | Dielectric composite material |
US8247079B2 (en) * | 2006-09-01 | 2012-08-21 | Momentive Performance Materials Inc. | Laminate containing a silylated polyurethane adhesive composition |
US7582691B2 (en) * | 2007-01-17 | 2009-09-01 | Sabic Innovative Plastics Ip B.V. | Poly(arylene ether) compositions and articles |
WO2011119216A2 (en) * | 2010-03-24 | 2011-09-29 | Dow Global Technologies Llc | Epoxy resin compositions comprising poly ( propylene oxide) polyol as toughening agent |
US9263314B2 (en) * | 2010-08-06 | 2016-02-16 | Brewer Science Inc. | Multiple bonding layers for thin-wafer handling |
US9269623B2 (en) * | 2012-10-25 | 2016-02-23 | Rohm And Haas Electronic Materials Llc | Ephemeral bonding |
US9315696B2 (en) | 2013-10-31 | 2016-04-19 | Dow Global Technologies Llc | Ephemeral bonding |
US9644118B2 (en) * | 2015-03-03 | 2017-05-09 | Dow Global Technologies Llc | Method of releasably attaching a semiconductor substrate to a carrier |
US9296915B1 (en) * | 2015-04-10 | 2016-03-29 | Dow Global Technologies Llc | Toughened arylcyclobutene polymers |
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CN106046225A (zh) | 2016-10-26 |
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TW201636386A (zh) | 2016-10-16 |
US9296915B1 (en) | 2016-03-29 |
JP2016199740A (ja) | 2016-12-01 |
US9518194B2 (en) | 2016-12-13 |
KR101791921B1 (ko) | 2017-11-02 |
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