WO2003072502A2 - Preparation of mixed-halogen halo-silanes - Google Patents
Preparation of mixed-halogen halo-silanes Download PDFInfo
- Publication number
- WO2003072502A2 WO2003072502A2 PCT/US2003/006101 US0306101W WO03072502A2 WO 2003072502 A2 WO2003072502 A2 WO 2003072502A2 US 0306101 W US0306101 W US 0306101W WO 03072502 A2 WO03072502 A2 WO 03072502A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- silane
- halo
- aryl
- halogen
- phenyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/12—Organo silicon halides
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B33/00—Silicon; Compounds thereof
- C01B33/08—Compounds containing halogen
- C01B33/107—Halogenated silanes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/12—Organo silicon halides
- C07F7/121—Preparation or treatment not provided for in C07F7/14, C07F7/16 or C07F7/20
- C07F7/123—Preparation or treatment not provided for in C07F7/14, C07F7/16 or C07F7/20 by reactions involving the formation of Si-halogen linkages
Definitions
- the present invention relates to the preparation of high-purity halo-silanes having two or more halogen moieties.
- mixed-halogen halo-silanes are useful sources of atomic silicon and halogens in a
- silane SiF 2 Cl 2
- chloro-trifluoro-silane SiF 3 Cl
- the mixed-halogen halo- silane must be high purity.
- high purity refers to a composition comprising at least 99 % by weight of one silane species and less than 0.5% by weight of non-silane impurities.
- elemental silicon may be treated with a halide gas, e.g., Cl 2 , and a halo-silane, e.g., SiF 4 , to produce, among other species, a mixed-halogen halo-silane, e.g., F 3 SiCl.
- a halide gas e.g., Cl 2
- a halo-silane e.g., SiF 4
- fluorine can replace chlorine, bromine, and iodine
- chlorine can replace bromine and iodine
- bromine can replace iodine
- halosilane species boil over a very narrow range, isolation of any one species to achieve high purity requires specialized equipment, such as a high theoretical plate distillation column,
- the present invention provides an efficient approach for preparing a mixed-halogen halo-silane with excellent yield and selectivity. Specifically, the approach involves first
- mixed-halogen halo-silane typically results in a distribution of mixed-halogen halo-silane species-i.e., silanes having different combinations
- aryl-halo-silane to prepare the final product offers a number of its own advantages.
- the process of the present invention provides for the predictable substitution of aryl groups by the lower bond strength halogens
- the aryl functionality of the aryl-halo-silane essentially determines the number of lower bond strength halogens on the end product. This is significant since silanes, which are functionalized in varying degrees with aryl groups, are readily isolated using traditional distillation techniques, especially compared to permutations of mixed-halogen halo-silanes which tend to have similar properties and, thus, are not readily separable.
- the purification can essentially be done before its preparation by readily isolating the particular aryl-halo-silane from which it is prepared. This way, the isolated aryl-halo-silane will contain the number of aryl groups corresponding to the desired number of lower bond strength halogens on the final product.
- halogen exchange can be a predictable, high
- the present invention allows for a highly reliable and efficient reaction to select the high-bond strength halogen of the mixed-halogen
- one aspect of the claimed invention is a process for preparing a mixed-
- the process comprises (a) providing an
- aryl-halo-silane comprising one or more first halogens and one or more aryl groups; and (b) substituting one or more of the aryl groups of said aryl-halo-silane with a second halogen
- aryl-halo-silane comprises providing an intermediate aryl-halo-silane having one more third
- providing said aryl-halo-silane further comprises isolating the aryl-halo-silane
- the present invention relates to a process for producing halo-silanes that contain two different species of halogen moieties (mixed-halogen halo-silanes) in high purity and in high
- the process comprises: (1) providing an aryl-halo-silane having one or more first halogens and one or more aryl groups, and (2) substituting at least some of the aryl groups with a second halogen which has an atomic number greater than that of the first halogen
- the first step in the process of the present invention is the provision of an aryl-halo-
- the step of providing an aryl-halo-silane comprises
- a an integer from 1 to 10;
- X is independently selected from F, Cl, and Br, and I; and aryl is an aryl or alkylaryl moiety.
- Preparation of the aryl-halo-silane is represented schematically in Equation (1) for a monosilane.
- (aryl)-M is an organometallic reagent.
- Equation (1) is art-recognized displacement of a halogen moiety from a silicon atom with the subsequent formation of an organo-silane by an organo-metallic
- organo-metal reagents for example, lithium reagents
- reaction is applicable to
- the starting material can be economically provided in a highly pure state.
- highly purified tetrachlorosilane silicon tetrachloride
- silicon tetrachloride is an article of commerce.
- the aryl moiety of the organometallic reagent can be any aromatic moiety, for example, phenyl, alkyl-substituted phenyl, biphenyl, aromatic heterocycles (e.g., pyrrolyl), and moieties based on fused aromatic ring compounds (e.g., napthyl).
- aromatic heterocycles e.g., pyrrolyl
- moieties based on fused aromatic ring compounds e.g., napthyl
- halogen halo-silane produced in step 2, above 1) the ability of the organo-silane bond to withstand subsequent processing conditions (e.g., as described below, the halogen
- silane adducts tend to boil over a wider temperature range and at a higher temperature.
- the aryl moiety of the aryl-halo-silane intermediate is liberated during aryl
- step 2 substitution (step 2) as the hydrogen adduct.
- a phenyl moiety is liberated as
- the halo-silane starting material can be chosen to yield a species which incorporates the halogen having the lowest atomic number of the halogens appearing in the
- the first reaction can utilize SiCl 4 as the starting material, and isolate the species
- the product is monofluoro substituted, the high-bond strength of the Si-F bond mitigates against use of tetrafluorosilane as a starting material from a standpoint of efficient utilization of the starting material and obtaining a narrow product distribution.
- the process of the present invention can include a step in which a chlorosilane is employed to provide an intermediate aryl-halo-silane that has chlorine substituents bonded to
- aryl-halo-silane such that it comprises the desired halogens.
- Z is a halogen other than X.
- X has an atomic number lower than Z.
- Z it may be preferable to
- n) where Y is a second halogen in place of the aryl group boil over a narrow range and, unlike a mixture of the cognate aryl species, cannot be separated in high purity by ordinary fractional distillation.
- the mixture of aryl-halo-silanes produced by the first reaction provides a precursor which is easily isolated in high purity, and can be used in the high specificity aryl substitution reaction (described below) to produce a high-purity mixed-halogen perhalogenated silane product.
- the mixed-halogen halo-silane is prepared substituting at least some of the aryl groups with a second halogen which has an atomic number greater than that of the first halogen substituents.
- the aryl groups of the silane of Formula (1) are substituted with second halogens to form the mixed-halogen halo-silane of Formula (2):
- X and Y are independently selected from F, Cl, and Br, and I such that the atomic number of X is less than Y;
- LA is a Lewis acid
- Equation (3) converts the isolated and purified intermediate aryl-halo- silane, whether directly from the reaction of Equation (1) or after having had the halogen
- aryl moieties are substituted by halogen moieties.
- the reaction comprising the method of conversion can be carried out using gas-phase reagents bubbled through the liquid starting
- Lewis acids catalyze the reaction comprising the method of converting aryl-silane
- Any Lewis acid which is capable of coordinating the hydrogen halide used in the reaction, and thereby promote dissociation of the hydrogen from the halide, can be used to catalyze the reaction.
- the Lewis acid can be
- Lewis acids are of
- MY Z where Y is selected from Cl, Br, and I, and M is a metal that can coordinate at least z+1 halogen moieties and has Lewis acid properties when coordinated with z halogen
- z is the number of halogen moeities cooridinated in the neutral metal complex.
- the most preferred Lewis acids are aluminum trihalides.
- the reaction can be run by contacting the two vapor
- the phase reactants over the Lewis acid (which is typically a solid).
- the hydrogen halide can be bubbled through the liquid, with the reactants contacting the Lewis acid present as a solid phase or dissolved in the liquid phase.
- the conditions in which the reactants are contacted are anhydrous.
- the phenyl-trichloro-silane starting material from which the phenyl-trifluoro-silane was prepared in the first example was obtained commercially as an article of commerce. All
- silane prepared in the first example was used in reactions of the second to fifth examples.
- the products of the examples were analyzed by gas chromatography/ mass spectrometry using a GC MS equipped with a DB-5 column.
- aryl-halo-silane a different pure species can be obtained.
- phenyl-trifluoro-silane prepared above was used as a starting material in the preparation of iodo-trifluoro-silane (Examples 2-4) and one
- Example 4 the reaction is conducted in the presence of pentane as a solvent.
- Example 5 was carried out at sub-ambient temperature.
- Anhydrous HI was produced in a gas generating apparatus comprising a flask equipped with a pressure equalized dropping funnel and a gas outlet by placing phosphorous pentoxide into
- the HI vapors thus generated were conducted from the gas generating apparatus to a reaction vessel consisting of a three neck flask equipped with a
- thermometer thermometer
- gas inlet tube thermometer
- dry ice condenser thermometer
- the flask contained a stirring device and the reaction mixture comprising phenyl-trifluoro-silane and aluminum triiodide, the
- the reaction mixture was analyzed for yield and purity of iodo-trifluoro-silane without separation of the components from the reaction mixture.
- reaction vessel described above was charged with 0.4 g of A1I 3 and 8.1 g of the phenyl-
- the HI generating apparatus described above was charged with 32.6 grams of phosphorous pentoxide in the flask and 22.5 g of aqueous HI in the dropping funnel.
- the reaction vessel described above was charged with 2.6 g of A1I 3 and 10.1 g of the phenyl-
- reaction vessel The reaction mixture was heated on a hot water bath with stirring to
- reaction mixture was held at this temperature for about 3 hours, during which the reaction mixture refluxed. At the end of this time, the reaction mixture was isolated and analyzed by GC/MS which indicated a yield, based on
- the reaction cylinder was then warmed to 38 degrees C by placing in a water bath and the valve opened, flash distilling the contents of the reaction cylinder into the receiving cylinder.
- the contents of the receiving cylinder were analyzed and found to be about 99.2% SiF 3 Cl with a yield of about 98 mole % based on the starting silane.
- aryl-halo-silane can be converted to a halo-silane having two different species of halogen moiety under a variety of conditions that yield a single product from the starting aryl-halo-silane.
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2003217799A AU2003217799A1 (en) | 2002-02-27 | 2003-02-27 | Preparation of mixed-halogen halo-silanes |
JP2003571213A JP2005519013A (en) | 2002-02-27 | 2003-02-27 | Preparation of mixed halogen halosilanes |
KR10-2004-7013486A KR20040096628A (en) | 2002-02-27 | 2003-02-27 | Preparation of Mixed-Halogen Halo-Silanes |
CA002477622A CA2477622A1 (en) | 2002-02-27 | 2003-02-27 | Preparation of mixed-halogen halo-silanes |
EP03713764A EP1480909A2 (en) | 2002-02-27 | 2003-02-27 | Preparation of mixed-halogen halo-silanes |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US35988402P | 2002-02-27 | 2002-02-27 | |
US60/359,884 | 2002-02-27 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2003072502A2 true WO2003072502A2 (en) | 2003-09-04 |
WO2003072502A3 WO2003072502A3 (en) | 2004-02-26 |
Family
ID=27766155
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2003/006101 WO2003072502A2 (en) | 2002-02-27 | 2003-02-27 | Preparation of mixed-halogen halo-silanes |
Country Status (8)
Country | Link |
---|---|
US (1) | US7030260B2 (en) |
EP (1) | EP1480909A2 (en) |
JP (1) | JP2005519013A (en) |
KR (1) | KR20040096628A (en) |
CN (1) | CN1646425A (en) |
AU (1) | AU2003217799A1 (en) |
CA (1) | CA2477622A1 (en) |
WO (1) | WO2003072502A2 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4837687B2 (en) * | 2008-02-04 | 2011-12-14 | 電気化学工業株式会社 | Chemical treatment method of chlorosilanes |
US8206676B2 (en) * | 2009-04-15 | 2012-06-26 | Air Products And Chemicals, Inc. | Method for making a chlorosilane |
JP6688513B2 (en) * | 2018-10-18 | 2020-04-28 | ヤマナカヒューテック株式会社 | Method for producing diiodosilane |
TWI798685B (en) * | 2020-04-24 | 2023-04-11 | 美商恩特葛瑞斯股份有限公司 | Method of preparing iodosilanes and compositions therefrom |
JP2023157339A (en) * | 2022-04-14 | 2023-10-26 | ヤマナカヒューテック株式会社 | Method for producing compound |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001097709A (en) * | 1999-10-01 | 2001-04-10 | Tori Chemical Kenkyusho:Kk | Production process for silicon trihalogenomonofluoride and silicon trihalogenomonofluoride |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2894012A (en) * | 1955-02-01 | 1959-07-07 | Metal & Thermit Corp | Grignard reactions in presence of cyclic ethers |
GB1238932A (en) | 1968-06-14 | 1971-07-14 | ||
JPS61117112A (en) | 1984-11-14 | 1986-06-04 | Central Glass Co Ltd | Preparation of fluorochlorosilane |
JPH0328371A (en) | 1989-06-23 | 1991-02-06 | Matsushita Electric Ind Co Ltd | Production of thin film |
-
2003
- 2003-02-27 WO PCT/US2003/006101 patent/WO2003072502A2/en not_active Application Discontinuation
- 2003-02-27 AU AU2003217799A patent/AU2003217799A1/en not_active Abandoned
- 2003-02-27 KR KR10-2004-7013486A patent/KR20040096628A/en not_active Application Discontinuation
- 2003-02-27 EP EP03713764A patent/EP1480909A2/en not_active Withdrawn
- 2003-02-27 US US10/377,367 patent/US7030260B2/en not_active Expired - Fee Related
- 2003-02-27 JP JP2003571213A patent/JP2005519013A/en not_active Withdrawn
- 2003-02-27 CA CA002477622A patent/CA2477622A1/en not_active Abandoned
- 2003-02-27 CN CNA038087677A patent/CN1646425A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001097709A (en) * | 1999-10-01 | 2001-04-10 | Tori Chemical Kenkyusho:Kk | Production process for silicon trihalogenomonofluoride and silicon trihalogenomonofluoride |
Non-Patent Citations (4)
Title |
---|
DATABASE CHEMABS [Online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; KURODA, KATSUHIKO ET AL: "Organic fluorine-silicon compounds. XI. Preparation and properties of silicon-functional phenylfluorosilanes and poly(phenylfluorosiloxane)" XP002265134 retrieved from STN Database accession no. 76:60125 & KOGYO KAGAKU ZASSHI , 74(10), 2132-7 CODEN: KGKZA7; ISSN: 0368-5462, 1971, * |
DATABASE CHEMABS [Online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; SURESH, B. S. ET AL: "Halogen exchange reactions of silicon tetrafluoride with phosphorus trichloride and phosphoryl chloride" XP002265135 retrieved from STN Database accession no. 103:204851 & JOURNAL OF FLUORINE CHEMISTRY , 29(4), 463-6 CODEN: JFLCAR; ISSN: 0022-1139, 1985, * |
PATENT ABSTRACTS OF JAPAN vol. 0103, no. 03 (C-378), 16 October 1986 (1986-10-16) & JP 61 117112 A (CENTRAL GLASS CO LTD), 4 June 1986 (1986-06-04) * |
PATENT ABSTRACTS OF JAPAN vol. 2000, no. 21, 3 August 2001 (2001-08-03) & JP 2001 097709 A (TORI CHEMICAL KENKYUSHO:KK), 10 April 2001 (2001-04-10) * |
Also Published As
Publication number | Publication date |
---|---|
CN1646425A (en) | 2005-07-27 |
CA2477622A1 (en) | 2003-09-04 |
US20040019231A1 (en) | 2004-01-29 |
EP1480909A2 (en) | 2004-12-01 |
US7030260B2 (en) | 2006-04-18 |
JP2005519013A (en) | 2005-06-30 |
WO2003072502A3 (en) | 2004-02-26 |
AU2003217799A1 (en) | 2003-09-09 |
KR20040096628A (en) | 2004-11-16 |
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