JP2018135516A5 - - Google Patents

Download PDF

Info

Publication number
JP2018135516A5
JP2018135516A5 JP2018028136A JP2018028136A JP2018135516A5 JP 2018135516 A5 JP2018135516 A5 JP 2018135516A5 JP 2018028136 A JP2018028136 A JP 2018028136A JP 2018028136 A JP2018028136 A JP 2018028136A JP 2018135516 A5 JP2018135516 A5 JP 2018135516A5
Authority
JP
Japan
Prior art keywords
group
carbon atoms
compound
mixed composition
different
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2018028136A
Other languages
Japanese (ja)
Other versions
JP2018135516A (en
JP6993894B2 (en
Filing date
Publication date
Application filed filed Critical
Publication of JP2018135516A publication Critical patent/JP2018135516A/en
Publication of JP2018135516A5 publication Critical patent/JP2018135516A5/ja
Application granted granted Critical
Publication of JP6993894B2 publication Critical patent/JP6993894B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Claims (9)

パーフルオロポリエーテル構造を有する1価の基と、加水分解性基とがケイ素原子に結合している第1の有機ケイ素化合物(A)と、
ケイ素原子に結合する加水分解性基を有し、パーフルオロポリエーテル構造を有さない第2の有機ケイ素化合物(B)と、
周期表第13族の金属元素を有する化合物の混合組成物であって、
前記第1の有機ケイ素化合物(A)が下記式(a3)または(a4)で表される化合物である混合組成物
Figure 2018135516
上記式(a3)中、R 30 は炭素数が2〜6のパーフルオロアルキル基であり、R 31 及びR 32 はそれぞれ独立していずれも炭素数が2〜6のパーフルオロアルキレン基であり、R 33 は炭素数が2〜6の3価の飽和炭化水素基であり、R 34 は炭素数が1〜3のアルキル基であり、h1は5〜70であり、h2は1〜5であり、h3は1〜10である。
Figure 2018135516
上記式(a4)中、R 40 は炭素数が2〜5のパーフルオロアルキル基であり、R 41 は炭素数が2〜5のパーフルオロアルキレン基であり、R 42 は炭素数2〜5のアルキレン基の水素原子の一部がフッ素に置換されたフルオロアルキレン基であり、R 43 、R 44 はそれぞれ独立に炭素数が2〜5のアルキレン基であり、R 45 はメチル基又はエチル基であり、k1、k2、k3はそれぞれ独立に1〜5の整数である。
A monovalent group having a perfluoropolyether structure, a first organosilicon compound (A) in which a hydrolyzable group is bonded to a silicon atom, and
A second organosilicon compound (B) having a hydrolyzable group bonded to a silicon atom and not having a perfluoropolyether structure,
A mixed composition of a compound having a periodic table Group 13 metal element,
A mixed composition in which the first organosilicon compound (A) is a compound represented by the following formula (a3) or (a4) .
Figure 2018135516
In the above formula (a3), R 30 is a perfluoroalkyl group having 2 to 6 carbon atoms, and R 31 and R 32 are independently perfluoroalkylene groups having 2 to 6 carbon atoms. R 33 is a trivalent saturated hydrocarbon group having 2 to 6 carbon atoms, R 34 is an alkyl group having 1 to 3 carbon atoms, h1 is 5 to 70, and h2 is 1 to 5. , H3 is 1-10.
Figure 2018135516
In the above formula (a4), R 40 is a perfluoroalkyl group having 2 to 5 carbon atoms , R 41 is a perfluoroalkylene group having 2 to 5 carbon atoms , and R 42 is a perfluoroalkylene group having 2 to 5 carbon atoms. A part of the hydrogen atom of the alkylene group is a fluoroalkylene group substituted with fluorine, R 43 and R 44 are independently alkylene groups having 2 to 5 carbon atoms, and R 45 is a methyl group or an ethyl group. Yes, k1, k2, and k3 are independently integers of 1 to 5.
周期表第13族の金属元素を有する化合物が、周期表第13族の金属元素を有する錯体である請求項1に記載の混合組成物。 The mixed composition according to claim 1, wherein the compound having a metal element of Group 13 of the periodic table is a complex having a metal element of Group 13 of the periodic table. 前記第2の有機ケイ素化合物(B)が、下記式(b1)で表される化合物を含む請求項1または2に記載の混合組成物。
Figure 2018135516
上記式(b1)中、
Rfb10は、1個以上の水素原子がフッ素原子に置換された炭素数1〜20のアルキル基又はフッ素原子であり、
b11、Rb12、Rb13、Rb14は、それぞれ独立して、水素原子又は炭素数が1〜4のアルキル基であり、Rb11が複数存在する場合は複数のRb11がそれぞれ異なっていてもよく、Rb12が複数存在する場合は複数のRb12がそれぞれ異なっていてもよく、Rb13が複数存在する場合は複数のRb13がそれぞれ異なっていてもよく、Rb14が複数存在する場合は複数のRb14がそれぞれ異なっていてもよく、
Rfb11、Rfb12、Rfb13、Rfb14は、それぞれ独立して、1個以上の水素原子がフッ素原子に置換された炭素数1〜20のアルキル基又はフッ素原子であり、Rfb11が複数存在する場合は複数のRfb11がそれぞれ異なっていてもよく、Rfb12が複数存在する場合は複数のRfb12がそれぞれ異なっていてもよく、Rfb13が複数存在する場合は複数のRfb13がそれぞれ異なっていてもよく、Rfb14が複数存在する場合は複数のRfb14がそれぞれ異なっていてもよく、
b15は、炭素数が1〜20のアルキル基であり、Rb15が複数存在する場合は複数のRb15がそれぞれ異なっていてもよく、
1は、−O−、−C(=O)−O−、−O−C(=O)−、−NR−、−NRC(=O)−、又は−C(=O)NR−であり、前記Rは水素原子、炭素数1〜4のアルキル基又は炭素数1〜4の含フッ素アルキル基であり、A1が複数存在する場合は複数のA1がそれぞれ異なっていてもよく、
2は、加水分解性基であり、A2が複数存在する場合は複数のA2がそれぞれ異なっていてもよく、
b11、b12、b13、b14、b15は、それぞれ独立して0以上100以下の整数であり、
cは1以上3以下の整数であり、
Rfb10−、−Si(A2c(Rb153-c、b11個の−{C(Rb11)(Rb12)}−、b12個の−{C(Rfb11)(Rfb12)}−、b13個の−{Si(Rb13)(Rb14)}−、b14個の−{Si(Rfb13)(Rfb14)}−、b15個の−A1−は、Rfb10−、−Si(A2c(Rb153-cが末端となり、ポリシロキサン構造を形成せず、パーフルオロポリエーテル構造を形成せず、かつ−O−が−O−乃至−Fと連結しない限り、任意の順で並んで結合する。
The mixed composition according to claim 1 or 2 , wherein the second organosilicon compound (B) contains a compound represented by the following formula (b1).
Figure 2018135516
In the above formula (b1),
Rf b10 is an alkyl group having 1 to 20 carbon atoms or a fluorine atom in which one or more hydrogen atoms are replaced with fluorine atoms.
R b11, R b12, R b13 , R b14 are each independently a hydrogen atom or a carbon number from 1 to 4 alkyl groups, if R b11 there are a plurality differ plurality of R b11 each may, if R b12 there are a plurality may be different plural R b12 each may be the case where R b13 there are a plurality of different plural R b13 are each if R b14 there are multiple May have different R b14s ,
Rf b11, Rf b12, Rf b13 , Rf b14 are each independently one or more alkyl group or a fluorine atom and having from 1 to 20 carbon atoms hydrogen atoms are substituted by fluorine atoms, Rf b11 multiple presence If you may be different plurality of Rf b11, respectively, differ if the Rf b12 there are a plurality may be different plurality of Rf b12, respectively, a plurality of Rf b13 If Rf b13 is present in plural even if well, if Rf b14 there are a plurality may be different plurality of Rf b14, respectively,
R b15 is an alkyl group having 1 to 20 carbon atoms, it may be the case where R b15 there are a plurality of different plural R b15 are each,
A 1 is −O−, −C (= O) −O−, −OC (= O) −, −NR−, −NRC (= O) −, or −C (= O) NR−. There, wherein R is a hydrogen atom, a fluorine-containing alkyl group of 1 to 4 alkyl groups or carbon atoms having 1 to 4 carbon atoms, if a 1 there are a plurality may be different plurality of a 1, respectively,
A 2 is a hydrolyzable group, if A 2 there are a plurality may be different plurality of A 2, respectively,
b11, b12, b13, b14, and b15 are each independently an integer of 0 or more and 100 or less.
c is an integer of 1 or more and 3 or less,
Rf b10 −, −Si (A 2 ) c (R b15 ) 3-c , b11 − {C (R b11 ) (R b12 )} −, b12 − {C (Rf b11 ) (Rf b12 ) } −, b13 − {Si (R b13 ) (R b14 )} −, b14 − {Si (Rf b13 ) (Rf b14 )} −, b15 − A 1 − are Rf b10 −, -Si (A 2 ) c (R b15 ) 3-c is the terminal, does not form a polysiloxane structure, does not form a perfluoropolyether structure, and -O- does not connect with -O- to -F. As long as they are combined side by side in any order.
前記金属の化合物がAl化合物である請求項1〜のいずれかに記載の混合組成物。 The mixed composition according to any one of claims 1 to 3 , wherein the metal compound is an Al compound. 前記金属の化合物が、Al錯体である請求項に記載の混合組成物。 The mixed composition according to claim 4 , wherein the metal compound is an Al complex. 前記第1の有機ケイ素化合物(A)及び第2の有機ケイ素化合物(B)の合計に対する前記金属の化合物の比が0.6〜5.0モル%である請求項1〜のいずれかに記載の混合組成物。 One of claims 1 to 5 , wherein the ratio of the compound of the metal to the total of the first organosilicon compound (A) and the second organosilicon compound (B) is 0.6 to 5.0 mol%. The mixed composition described. 前記第1の有機ケイ素化合物(A)及び第2の有機ケイ素化合物(B)の合計に対する前記金属の化合物の比が0.1〜2.0質量%である請求項1〜のいずれかに記載の混合組成物。 One of claims 1 to 6 , wherein the ratio of the compound of the metal to the total of the first organosilicon compound (A) and the second organosilicon compound (B) is 0.1 to 2.0% by mass. The mixed composition described. 請求項1〜のいずれかに記載の混合組成物を硬化してなる膜を備える被覆体。 A coating body comprising a film obtained by curing the mixed composition according to any one of claims 1 to 7 . 前記混合組成物を常温で硬化させることを特徴とする、請求項に記載の被覆体の製造方法。 The method for producing a coating body according to claim 8 , wherein the mixed composition is cured at room temperature.
JP2018028136A 2017-02-22 2018-02-20 Composition Active JP6993894B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2017031513 2017-02-22
JP2017031513 2017-02-22

Publications (3)

Publication Number Publication Date
JP2018135516A JP2018135516A (en) 2018-08-30
JP2018135516A5 true JP2018135516A5 (en) 2021-02-12
JP6993894B2 JP6993894B2 (en) 2022-01-14

Family

ID=63252597

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2018028136A Active JP6993894B2 (en) 2017-02-22 2018-02-20 Composition

Country Status (5)

Country Link
JP (1) JP6993894B2 (en)
KR (1) KR20190116476A (en)
CN (1) CN110268018A (en)
TW (1) TWI762582B (en)
WO (1) WO2018155325A1 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20200078633A (en) * 2017-11-07 2020-07-01 스미또모 가가꾸 가부시키가이샤 Composition
JP2022017617A (en) * 2018-11-13 2022-01-26 Agc株式会社 Fluorine-containing ether composition, coating liquid, article and production method thereof
EP3950780A4 (en) * 2019-03-29 2022-12-21 Daikin Industries, Ltd. Fluoropolyether-group-containing compound
CN116507682A (en) * 2021-01-28 2023-07-28 大金工业株式会社 Liquid composition for surface treatment

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4580774B2 (en) * 2004-02-16 2010-11-17 富士フイルム株式会社 Antireflection film, polarizing plate using the same, and display device using them
US7695781B2 (en) * 2004-02-16 2010-04-13 Fujifilm Corporation Antireflective film, polarizing plate including the same, image display unit including the same and method for producing antireflective film
JP5131840B2 (en) 2007-07-03 2013-01-30 信越化学工業株式会社 COATING COMPOSITION AND HIGH DRILLING FILM USING THE COMPOSITION
JP5630985B2 (en) 2009-10-27 2014-11-26 信越化学工業株式会社 Antifouling substrate manufacturing method and antifouling article
JP5459232B2 (en) 2010-01-19 2014-04-02 信越化学工業株式会社 Addition-curing fluoropolyether adhesive composition
WO2011125753A1 (en) * 2010-04-02 2011-10-13 株式会社カネカ Curable resin composition, curable resin composition tablet, molded body, semiconductor package, semiconductor component and light emitting diode
JP6060698B2 (en) * 2013-01-23 2017-01-18 信越化学工業株式会社 Curable resin composition and coated article
JP2016020407A (en) * 2014-07-11 2016-02-04 信越化学工業株式会社 Method for curing fluorine-containing organic silicon compound, method for producing cured film, composition including fluorine-containing organic silicon compound, and surface-treated article with cured product of the composition
JP6705752B2 (en) * 2014-11-12 2020-06-03 住友化学株式会社 Water- and oil-repellent coating composition and transparent film
EP3334541B1 (en) * 2015-08-10 2021-12-29 Essilor International Article having a nanotextured surface with hydrophobic properties

Similar Documents

Publication Publication Date Title
JP2018135516A5 (en)
JP2013254069A5 (en)
JP2015062072A5 (en)
JP2017125193A5 (en)
JP2017125092A5 (en)
RU2009140077A (en) COATING COMPOSITION CONTAINING SILICONE RESIN AND COATED SUPPORT
JP2011145659A5 (en)
JP2015181191A5 (en)
JP2013170170A5 (en)
JP2009544816A5 (en)
JP2012237994A5 (en)
EP2650399A3 (en) High temperature atomic layer deposition of silicon oxide thin films
JP2012237993A5 (en)
JP2012098720A5 (en)
JP2008545631A5 (en)
JP2007502814A5 (en)
JP2014515050A5 (en)
JP2010004055A5 (en)
JP2008280420A5 (en)
JP2019011463A5 (en)
JP2017051113A5 (en)
JP2019084827A5 (en)
JP2014178672A5 (en)
JP2016011993A5 (en)
JP2007004113A5 (en)