JPS6147735A - 有機窒化ホウ素重合体の製造法 - Google Patents
有機窒化ホウ素重合体の製造法Info
- Publication number
- JPS6147735A JPS6147735A JP59168454A JP16845484A JPS6147735A JP S6147735 A JPS6147735 A JP S6147735A JP 59168454 A JP59168454 A JP 59168454A JP 16845484 A JP16845484 A JP 16845484A JP S6147735 A JPS6147735 A JP S6147735A
- Authority
- JP
- Japan
- Prior art keywords
- boron nitride
- group
- organic boron
- aryl
- polymer
- 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
Links
- 229910052582 BN Inorganic materials 0.000 title claims abstract description 25
- 229920000642 polymer Polymers 0.000 title claims abstract description 15
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 title abstract description 23
- -1 amine compound Chemical class 0.000 claims abstract description 24
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 15
- 125000003118 aryl group Chemical group 0.000 claims abstract description 13
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims abstract description 6
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 4
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 3
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 7
- 238000006116 polymerization reaction Methods 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 125000001302 tertiary amino group Chemical group 0.000 claims description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 2
- 239000000203 mixture Substances 0.000 abstract description 5
- 229920006037 cross link polymer Polymers 0.000 abstract description 3
- 238000000465 moulding Methods 0.000 abstract description 2
- 230000000379 polymerizing effect Effects 0.000 abstract description 2
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 230000004580 weight loss Effects 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 5
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000000835 fiber Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 238000010304 firing Methods 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- ORKQJTBYQZITLA-UHFFFAOYSA-N 4-octylaniline Chemical compound CCCCCCCCC1=CC=C(N)C=C1 ORKQJTBYQZITLA-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 238000001354 calcination Methods 0.000 description 2
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000013585 weight reducing agent Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- 101100294102 Caenorhabditis elegans nhr-2 gene Proteins 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- BGECDVWSWDRFSP-UHFFFAOYSA-N borazine Chemical group B1NBNBN1 BGECDVWSWDRFSP-UHFFFAOYSA-N 0.000 description 1
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 101150009274 nhr-1 gene Proteins 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
- C08G79/08—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule a linkage containing boron
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B21/00—Nitrogen; Compounds thereof
- C01B21/06—Binary compounds of nitrogen with metals, with silicon, or with boron, or with carbon, i.e. nitrides; Compounds of nitrogen with more than one metal, silicon or boron
- C01B21/064—Binary compounds of nitrogen with metals, with silicon, or with boron, or with carbon, i.e. nitrides; Compounds of nitrogen with more than one metal, silicon or boron with boron
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/58—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides
- C04B35/583—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on boron nitride
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/62227—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products obtaining fibres
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/38—Boron-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2002/00—Crystal-structural characteristics
- C01P2002/80—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70
- C01P2002/82—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70 by IR- or Raman-data
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Inorganic Chemistry (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59168454A JPS6147735A (ja) | 1984-08-11 | 1984-08-11 | 有機窒化ホウ素重合体の製造法 |
| GB08519708A GB2163761B (en) | 1984-08-11 | 1985-08-06 | Process of preparing organoboron nitride polymer |
| US06/762,935 US4731437A (en) | 1984-08-11 | 1985-08-06 | Process of preparing organoboron nitride polymer |
| DE19853528394 DE3528394A1 (de) | 1984-08-11 | 1985-08-07 | Verfahren zur herstellung von organobornitridpolymeren |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59168454A JPS6147735A (ja) | 1984-08-11 | 1984-08-11 | 有機窒化ホウ素重合体の製造法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6147735A true JPS6147735A (ja) | 1986-03-08 |
| JPH0363976B2 JPH0363976B2 (en]) | 1991-10-03 |
Family
ID=15868404
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59168454A Granted JPS6147735A (ja) | 1984-08-11 | 1984-08-11 | 有機窒化ホウ素重合体の製造法 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US4731437A (en]) |
| JP (1) | JPS6147735A (en]) |
| DE (1) | DE3528394A1 (en]) |
| GB (1) | GB2163761B (en]) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5061469A (en) * | 1988-05-19 | 1991-10-29 | Mitsubishi Kasei Corporation | Process for producing shaped boron nitride product |
| JP2008019436A (ja) * | 2007-07-02 | 2008-01-31 | Mitsubishi Electric Corp | 低誘電率材料形成用原料 |
| JP2008239787A (ja) * | 2007-03-27 | 2008-10-09 | National Institute Of Advanced Industrial & Technology | ボラジン・ジアミン系重合体及びそのための重合性組成物、並びにその製造方法 |
| JP2008239796A (ja) * | 2007-03-27 | 2008-10-09 | National Institute Of Advanced Industrial & Technology | ボラジン・ジアミン系ポリマー薄膜形成用組成物及びボラジン・ジアミン系ポリマー薄膜の製造方法 |
| JP2012012607A (ja) * | 2011-07-14 | 2012-01-19 | Mitsubishi Electric Corp | 低誘電率材料形成用原料 |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4906763A (en) * | 1987-02-13 | 1990-03-06 | Paciorek Kazimiera J L | Boron nitride preceramic polymers |
| FR2620454B1 (fr) * | 1987-09-11 | 1989-12-22 | Rhone Poulenc Chimie | Polymeres a base de bore et d'azote utilisables notamment pour la fabrication de produits et articles ceramiques a base de nitrure de bore, ainsi que leur procede de preparation |
| FR2620455B1 (fr) * | 1987-09-11 | 1989-12-22 | Rhone Poulenc Chimie | Polymeres a base de bore et d'azote, leur procede de preparation et leur utilisation dans la fabrication de produits et articles ceramiques a base de nitrure de bore |
| FR2620443B1 (fr) * | 1987-09-11 | 1989-12-22 | Rhone Poulenc Chimie | Nouveaux composes a base de nitrure de bore |
| US5045399A (en) * | 1988-01-22 | 1991-09-03 | Ethyl Corporation | Organoborosilazane polymers |
| US4865830A (en) * | 1988-01-27 | 1989-09-12 | E. I. Du Pont De Nemours And Company | Gas phase preparation of aluminum nitride |
| FR2637602B1 (fr) * | 1988-10-06 | 1990-12-14 | Rhone Poulenc Chimie | Procede de synthese de polymeres a base de bore et d'azote precurseurs de nitrure de bore et produits susceptibles d'etre ainsi obtenus |
| FR2637603B1 (fr) * | 1988-10-06 | 1992-06-12 | Rhone Poulenc Chimie | Polymeres a base de bore et d'azote, leur procede de preparation et leur utilisation comme precurseurs de nitrure de bore |
| US5204295A (en) * | 1989-02-17 | 1993-04-20 | University Of New Mexico | Precursors for boron nitride coatings |
| FR2643358B1 (fr) * | 1989-02-20 | 1991-11-22 | Rhone Poulenc Chimie | Procede de preparation de nitrure de bore |
| US5128286A (en) * | 1989-06-20 | 1992-07-07 | Tonen Corporation | Boron-containing, silicon nitride-based ceramic shaped body |
| FR2650832B1 (fr) * | 1989-08-10 | 1991-11-22 | Rhone Poulenc Chimie | Precurseur ceramique organometallique a base de bore, d'azote et de silicium |
| FR2659321B1 (fr) * | 1990-03-12 | 1992-05-22 | Rhone Poulenc Chimie | Procede de revetements en ceramique de pieces a base de carbone. |
| FR2661181B1 (fr) * | 1990-04-20 | 1992-06-19 | Rhone Poulenc Chimie | Procede de reticulation de polymeres a base de bore et d'azote, notamment pour l'obtention de fibres ceramiques. |
| FR2678621A1 (fr) * | 1991-07-02 | 1993-01-08 | Atochem | Procede de preparation de ceramiques en nitrure de bore et de leurs precurseurs a partir de derives de l'hydrazine et les precurseurs ainsi mis en óoeuvre. |
| FR2757848B1 (fr) * | 1996-12-27 | 1999-03-26 | Europ Propulsion | Preformes fibreuses gainees d'un revetement bn original, composites les incorporant et leurs preparations |
| JP3778045B2 (ja) * | 2001-10-09 | 2006-05-24 | 三菱電機株式会社 | 低誘電率材料の製造方法および低誘電率材料、並びにこの低誘電率材料を用いた絶縁膜および半導体装置 |
| KR102611514B1 (ko) | 2016-11-25 | 2023-12-06 | 엘지디스플레이 주식회사 | 접촉 감응 소자 및 이를 포함하는 표시 장치 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB857176A (en) * | 1958-06-30 | 1960-12-29 | United States Borax Chem | Preparation of aminoboranes |
| US3052641A (en) * | 1959-08-03 | 1962-09-04 | United States Borax Chem | Boron-nitrogen polymers |
| US3068182A (en) * | 1959-08-24 | 1962-12-11 | United States Borax Chem | Preparation of aminoboranes |
| GB975451A (en) * | 1960-03-11 | 1964-11-18 | Napier & Son Ltd | Amino borazoles and their polymerization products |
| GB1018031A (en) * | 1961-02-16 | 1966-01-26 | Nat Res Dev | Polymers containing borazole rings |
| JPS60120725A (ja) * | 1983-12-05 | 1985-06-28 | Shin Etsu Chem Co Ltd | 有機金属共重合体およびその製造方法 |
-
1984
- 1984-08-11 JP JP59168454A patent/JPS6147735A/ja active Granted
-
1985
- 1985-08-06 US US06/762,935 patent/US4731437A/en not_active Expired - Fee Related
- 1985-08-06 GB GB08519708A patent/GB2163761B/en not_active Expired
- 1985-08-07 DE DE19853528394 patent/DE3528394A1/de active Granted
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5061469A (en) * | 1988-05-19 | 1991-10-29 | Mitsubishi Kasei Corporation | Process for producing shaped boron nitride product |
| JP2008239787A (ja) * | 2007-03-27 | 2008-10-09 | National Institute Of Advanced Industrial & Technology | ボラジン・ジアミン系重合体及びそのための重合性組成物、並びにその製造方法 |
| JP2008239796A (ja) * | 2007-03-27 | 2008-10-09 | National Institute Of Advanced Industrial & Technology | ボラジン・ジアミン系ポリマー薄膜形成用組成物及びボラジン・ジアミン系ポリマー薄膜の製造方法 |
| JP2008019436A (ja) * | 2007-07-02 | 2008-01-31 | Mitsubishi Electric Corp | 低誘電率材料形成用原料 |
| JP2012012607A (ja) * | 2011-07-14 | 2012-01-19 | Mitsubishi Electric Corp | 低誘電率材料形成用原料 |
Also Published As
| Publication number | Publication date |
|---|---|
| US4731437A (en) | 1988-03-15 |
| GB8519708D0 (en) | 1985-09-11 |
| GB2163761A (en) | 1986-03-05 |
| DE3528394A1 (de) | 1986-02-20 |
| GB2163761B (en) | 1988-04-07 |
| DE3528394C2 (en]) | 1990-05-23 |
| JPH0363976B2 (en]) | 1991-10-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS6147735A (ja) | 有機窒化ホウ素重合体の製造法 | |
| US4340619A (en) | Process for the preparation of poly(disilyl)silazane polymers and the polymers therefrom | |
| US4414403A (en) | Branched polycarbosilanes and their use in the production of silicon carbide | |
| US4783516A (en) | Polysilane precursors containing olefinic groups for silicon carbide | |
| JPS60226890A (ja) | プレセラミツク有機シラザン重合体 | |
| JPS62225534A (ja) | ポリシラザン類の製造方法 | |
| CN101274941B (zh) | 一种聚硼硅氮烷先驱体制备方法 | |
| EP0490614B1 (en) | Preparation of titanium nitride from organometallic precursors | |
| JPS63309526A (ja) | 新規ポリシラザン及びその製造方法 | |
| KR20010041184A (ko) | 불포화 유기 말단기를 갖는 실릴 및 실록실로 치환된 카보레인 조성물 | |
| JPS6189230A (ja) | ポリオルガノヒドロシラザンの製造方法 | |
| JPS63267791A (ja) | 環状シルエチニルポリマーの製造方法 | |
| EP0139257A2 (en) | Process for the manufacture of silicon carbide | |
| US3354098A (en) | Elastomeric silazane polymers and process for preparing the same | |
| JPS584732B2 (ja) | 耐加水分解性、耐熱性に優れたボロシロキサンポリマ−の製造方法 | |
| JP2002155144A (ja) | ボラジン含有ケイ素系共重合ポリマー及びその薄膜の製造方法 | |
| CN101585850A (zh) | 一种含硅芳香氰酸酯单体及其制备方法 | |
| JPS61281126A (ja) | ラクタムを重合せさる方法及びそれより得られる生成物 | |
| Tomita et al. | Rearrangements versus ligand exchange reactions of organocobalt polymer having cobaltacyclopentadiene moieties in the main chain | |
| US5149764A (en) | Substituted silyl-terminated compounds and polymers thereof | |
| JPH04227637A (ja) | 特にセラミック繊維の製造のための硼素及び窒素を主体としたポリマーの架橋方法 | |
| US5075475A (en) | Aromatic polyimide silanol compounds, precursors and polymers thereof | |
| US3230252A (en) | Synthesis of phenylchlorotetra-phosphonitriles | |
| Pan et al. | Phenylated Group 13/15 Compounds: Convenient Precursors to Phase Pure Gallium Arsenide and Gallium Phosphide | |
| US3531443A (en) | Poly-m- and p-carboranylenedisulfides |