JPS62167786A - シラン試薬、それらの製法及び変性無機材料 - Google Patents

シラン試薬、それらの製法及び変性無機材料

Info

Publication number: JPS62167786A
Authority: JP; Japan
Prior art keywords: formulas; formula; group; tables; following general
Prior art date: 1985-11-11
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.): Pending

Application number

JP26572386A

Other languages

English (en)

Japanese (ja)

Inventor

ヤロスラブ　カホベツ

ベドジーフ　ポルスフ

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Czech Academy of Sciences CAS

Original Assignee

Czech Academy of Sciences CAS

Priority date (The priority date 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 date listed.)

1985-11-11

Filing date

1986-11-10

Publication date

1987-07-24

1986-11-10 Application filed by Czech Academy of Sciences CAS filed Critical Czech Academy of Sciences CAS

1987-07-24 Publication of JPS62167786A publication Critical patent/JPS62167786A/ja

Status Pending legal-status Critical Current

Links

239000003153 chemical reaction reagent Substances 0.000 title claims description 29
229910010272 inorganic material Inorganic materials 0.000 title claims description 16
239000011147 inorganic material Substances 0.000 title claims description 16
229910000077 silane Inorganic materials 0.000 title claims description 13
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 title claims description 12
238000004519 manufacturing process Methods 0.000 title claims description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 16
239000000126 substance Substances 0.000 claims description 11
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 9
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 8
238000000034 method Methods 0.000 claims description 7
238000002360 preparation method Methods 0.000 claims description 6
239000000377 silicon dioxide Substances 0.000 claims description 5
150000001875 compounds Chemical class 0.000 claims description 4
239000011521 glass Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 4
239000011148 porous material Substances 0.000 claims description 4
239000004408 titanium dioxide Substances 0.000 claims description 4
GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 claims description 3
235000012239 silicon dioxide Nutrition 0.000 claims description 3
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical group [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 claims 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
239000000463 material Substances 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 8
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
230000007062 hydrolysis Effects 0.000 description 5
238000006460 hydrolysis reaction Methods 0.000 description 5
239000000741 silica gel Substances 0.000 description 5
229910002027 silica gel Inorganic materials 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 4
125000003545 alkoxy group Chemical group 0.000 description 4
150000004819 silanols Chemical class 0.000 description 4
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical class NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
125000000524 functional group Chemical group 0.000 description 3
NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical group OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
239000000203 mixture Substances 0.000 description 3
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
239000005725 8-Hydroxyquinoline Substances 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
239000012736 aqueous medium Substances 0.000 description 2
239000002131 composite material Substances 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
238000004811 liquid chromatography Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000012986 modification Methods 0.000 description 2
229960003540 oxyquinoline Drugs 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
239000005373 porous glass Substances 0.000 description 2
MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 2
150000004756 silanes Chemical class 0.000 description 2
150000004760 silicates Chemical class 0.000 description 2
238000003756 stirring Methods 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
BDDLHHRCDSJVKV-UHFFFAOYSA-N 7028-40-2 Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O BDDLHHRCDSJVKV-UHFFFAOYSA-N 0.000 description 1
101100234244 Arabidopsis thaliana KDTA gene Proteins 0.000 description 1
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
102000004190 Enzymes Human genes 0.000 description 1
108090000790 Enzymes Proteins 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241001474791 Proboscis Species 0.000 description 1
241000283984 Rodentia Species 0.000 description 1
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
125000005370 alkoxysilyl group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000013040 bath agent Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
239000013522 chelant Substances 0.000 description 1
230000009920 chelation Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
-1 chlorosilyl Chemical group 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000010411 cooking Methods 0.000 description 1
239000007822 coupling agent Substances 0.000 description 1
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000002895 emetic Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000003292 glue Substances 0.000 description 1
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
239000010931 gold Substances 0.000 description 1
229910052737 gold Inorganic materials 0.000 description 1
238000007210 heterogeneous catalysis Methods 0.000 description 1
150000002431 hydrogen Chemical group 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000003993 interaction Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000002609 medium Substances 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
150000003961 organosilicon compounds Chemical group 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 description 1
239000002904 solvent Substances 0.000 description 1
230000002269 spontaneous effect Effects 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
239000010936 titanium Substances 0.000 description 1

Landscapes

Surface Treatment Of Glass (AREA)
Solid-Sorbent Or Filter-Aiding Compositions (AREA)

JP26572386A 1985-11-11 1986-11-10 シラン試薬、それらの製法及び変性無機材料 Pending JPS62167786A (ja)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
CS8111-85		1985-11-11
CS858111A CS256456B1 (cs)	1985-11-11	1985-11-11	Silanová činidla obsahující chemicky vázané komplexonové seskupení
CS248-86		1986-01-10

Publications (1)

Publication Number	Publication Date
JPS62167786A true JPS62167786A (ja)	1987-07-24

Family

ID=5431269

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP26572386A Pending JPS62167786A (ja)	1985-11-11	1986-11-10	シラン試薬、それらの製法及び変性無機材料

Country Status (2)

Country	Link
JP (1)	JPS62167786A (cs)
CS (1)	CS256456B1 (cs)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2010535725A (ja) *	2007-08-06	2010-11-25	マックス−プランク−ゲゼルシャフトツールフォーデルングデルヴィッセンシャフテンエー．ヴェー．	固定金属イオンクロマトグラフィー（ｉｍａｃ）のためのキレート基の固定

1985
- 1985-11-11 CS CS858111A patent/CS256456B1/cs unknown
1986
- 1986-11-10 JP JP26572386A patent/JPS62167786A/ja active Pending

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2010535725A (ja) *	2007-08-06	2010-11-25	マックス−プランク−ゲゼルシャフトツールフォーデルングデルヴィッセンシャフテンエー．ヴェー．	固定金属イオンクロマトグラフィー（ｉｍａｃ）のためのキレート基の固定

Also Published As

Publication number	Publication date
CS811185A1 (en)	1987-09-17
CS256456B1 (cs)	1988-04-15

Publication	Publication Date	Title
US4835269A (en)	1989-05-30	Silane reagents containing a complexon group
DE3606262C2 (cs)	1991-10-31
JPS6330311A (ja)	1988-02-09	変性シリカ及びその製法
JPS59137493A (ja)	1984-08-07	ＳｉＣ‐結合した無水コハク酸基を有するシランの製法
JPS62167786A (ja)	1987-07-24	シラン試薬、それらの製法及び変性無機材料
JPS63502116A (ja)	1988-08-18	接着促進剤として有効な多機能アミノ・ジルコニウム・アルミニウム金属有機合成物
JP7182750B1 (ja)	2022-12-02	ベタイン基含有有機ケイ素化合物およびその成形物と製造方法
JPS63243088A (ja)	1988-10-07	スルホン化オルガノシリコーン化合物の製造方法
US4562251A (en)	1985-12-31	Agarose derivatives of amino phenyl boronic acid
KR100657907B1 (ko)	2006-12-14	신규한 링커 화합물, 상기 화합물이 코팅되어 있는 기판,상기 화합물을 이용하여 마이크로어레이를 제조하는 방법및 그에 의하여 제조된 마이크로어레이
DE69309993T2 (de)	1997-08-28	Fluor enthaltende Organosiliziumverbindung und Verfahren zu deren Herstellung
JPS6264801A (ja)	1987-03-23	セルロ−ス系カルバメ−ト誘導体
JPH04235993A (ja)	1992-08-25	有機ケイ素化合物
US20230098702A1 (en)	2023-03-30	Amphoteric fluorescent substance capable of being attached to biomaterials
JP3288747B2 (ja)	2002-06-04	トリメチルシリルシアニドの製造法
JPH04252228A (ja)	1992-09-08	シリコーン含有エポキシ化合物及びその製法
US4778888A (en)	1988-10-18	Boron containing 1,3,5-triazines
JPS62103064A (ja)	1987-05-13	４，５，６または７−位を介して結合したインド−ルまたはその誘導体、およびその製造方法並びその使用方法
JP3821191B2 (ja)	2006-09-13	有機珪素化合物及びその製造方法
JPS6233189A (ja)	1987-02-13	置換シリルアルキルエステル基含有セルロ−ス誘導体とその製造方法
JPS6377886A (ja)	1988-04-08	有機けい素化合物
KR100460177B1 (ko)	2004-12-08	탄수화물칩 제작방법
JP3300405B2 (ja)	2002-07-08	グアニジン化合物のケイ酸塩の製造方法
KR101946488B1 (ko)	2019-02-11	링커 화합물 및 이의 제조방법
JPH02240086A (ja)	1990-09-25	オルトリチオ置換フェニルシラン化合物の製造方法

JPS62167786A - シラン試薬、それらの製法及び変性無機材料 - Google Patents

Info

Links

Landscapes

Applications Claiming Priority (3)

Publications (1)

Family

ID=5431269

Family Applications (1)

Country Status (2)

Cited By (1)

Cited By (1)

Also Published As

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