CN1844126A - Process for preparing amino phenyl silsesquioxane - Google Patents
Process for preparing amino phenyl silsesquioxane Download PDFInfo
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- CN1844126A CN1844126A CN 200610080871 CN200610080871A CN1844126A CN 1844126 A CN1844126 A CN 1844126A CN 200610080871 CN200610080871 CN 200610080871 CN 200610080871 A CN200610080871 A CN 200610080871A CN 1844126 A CN1844126 A CN 1844126A
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Abstract
This invention belonging to nano material technology is the synthesis of eight-amino-benzene cage model sesquialter siloxane. The previous method adopts aminic acid as hydrogen donor and Pd/C catalysis system. Our method is as followings:mix the eight-nitrobenzene cage model sesquialter siloxane, solvent and Fe/C catalysis in the weight propotion of 10:50-200:2-10,stiring in the air or nitrogen at 50- 100deg C; add 2-4 weight folds hydrazine hydrate or phenylhydrazine into eight-nitrobenzene cage model sesquialter siloxane, react for 2-12 hours; cool to ambience temperature, filter and add acetic ester for extraction, wait to layers; Get organic facies and precipitate in ligarine,obtain white sediment after separation and dry. This invention is advantageous in cheap, stable and long-term active Fe/C catalysis system, is advantageous in production efficiency.
Description
Technical field
The present invention relates to a kind of synthetic method of silsesquioxane.More particularly, relate to the synthetic method of eight aminophenyl cage-type silsesquioxanes, the metal nanometer material technical field.
Background technology
Silsesquioxane is that a class formation skeleton symbol is (RSiO
1.5)
nCompound.Mainly contain different types of structure such as random, trapezoidal, bridge shape and cage type.Wherein cage structure is to study maximum class silsesquioxanes at present.
Eight aminophenyl cage-type silsesquioxanes are hexahedrons that each face all is made of the silica octatomic ring, wherein connect eight aminophenyl cage modle groups respectively at place, polyhedral eight Siliciumatom summits.The organo-functional group that the structural symmetry of this macromonomer is very strong, have a plurality of chemical property, simultaneously, its three-dimensional dimension is about 1.5nm, and can make with silicon-dioxide from the it is the Organic of core.In addition, because its amino has very big reactive behavior, can react with many groups such as epoxy, acid anhydrides, can further carry out chemically modified to phenyl silsesquioxane, preparation is such as various functional materialss such as high temperature resistant, luminous.
Cagelike silsesquioxane can be incorporated in the polymeric matrix by the method for copolymerization, grafting and blend, obtains the macromolecular material of specified property.Polymkeric substance is after eight aminophenyl cage-type silsesquioxane modifications, compare with matrix polymer, combustionproperty and thermal conducting rate descend, and the perviousness of scale resistance, gas, second-order transition temperature (Tg), thermal distortion and melt strength, modulus all increase, and be especially remarkable with the increase of modulus.The tensile property of very valuable is material is constant substantially, and the tensile property of the nano composite material that is made by other method generally descends.The researchist of U.S. Air Force Lab. has done many work in this respect, is referred to as ' follow-on material '.The research of this material is expected to make existing polymer to enter the field of more renewals.
It mainly is at first to prepare the silsesquioxane that contains phenyl that preparation at present contains the method for aminophenyl cage-type silsesquioxane, through nitrated, obtains the silsesquioxane of nitrobenzene-containing base; Pass through catalytic reduction again, obtain containing the aminophenyl cage-type silsesquioxane.
The fracture of key takes place under alkaline condition easily because of siloxane bond, cause the structure deteriorate of silsesquioxane, the method that the preparation of therefore present bibliographical information contains the aminophenyl cage-type silsesquioxane all adopts the hydrogen transference hydrogenation method (J.Am.Chem.Soc. of U.S. Laine research group in report in 2000,2001,123,12416), promptly be hydrogen donor with formic acid, under the Pd/C catalyst action, reduce nitro, preparation aminophenyl cage-type silsesquioxane.
At present, relevant silsesquioxane preparation mainly contains in the patent of China: a kind of aminophenyl cage-type silsesquioxane and preparation method thereof (publication number: CN1648130,2005, August 3, Li Qifang Zhang Lipei), adopts the hydrogen transference hydrogenation method to prepare the aminophenyl cage-type silsesquioxane, the result shows that this product can be added in the Resins, epoxy, improves material property.But its preparation method still is hydrogen donor with formic acid, adopts the Pd/C catalyst system.
Summary of the invention
The objective of the invention is to propose a kind of synthetic method of eight aminophenyl cage-type silsesquioxanes.This method is to adopt alkaline reducing agent hydrazine hydrate or phenylhydrazine, and the nitro of reduction eight nitrophenyl silsesquioxanes obtains the silsesquioxane that corresponding eight aminophenyl cage modles are rolled into a ball under catalyst action, and does not destroy the cagelike structure of siloxanes.Its advantage is owing to used hydrazine hydrate to be reductive agent, and corresponding catalyst system (Fe/C) raw material is easy to get, inexpensive, and catalytic activity is stable, is difficult for inactivation, and the product yield height.Therefore, can obviously reduce the production cost of eight aminophenyl cage-type silsesquioxanes.
The invention provides a kind of preparation method of eight aminophenyl cage-type silsesquioxanes, it is characterized in that, may further comprise the steps:
1) is that 10: 50～200: 2～10 eight nitrophenyl cage-type silsesquioxanes, solvent and Fe/C catalyzer stir in air or nitrogen atmosphere with weight ratio, is warming up to 50～100 ℃;
2) weight ratio according to eight nitrophenyl cage-type silsesquioxanes and reductive agent is 1: 2～8 adding hydrazine hydrate or phenylhydrazine reductive agents, reacts 2～12 hours;
3) reduce to room temperature after the reaction, filter, add ethyl acetate extraction, standing demix;
4) get organic phase behind the standing demix, in sherwood oil, precipitate, through separating, obtaining white precipitate after the drying, i.e. eight aminophenyl silsesquioxanes.
It is 50～100% hydrazine hydrate or phenylhydrazine that hydrazine class reductive agent of the present invention is included as mass concentration.
The weight ratio of raw materials used eight nitrophenyl cage-type silsesquioxanes of the present invention and reductive agent is 1: 2～8.
Solvent of the present invention is ether, sulfone, acid amides and aromatic compound aromatics, for example tetrahydrofuran (THF), dioxane, dimethyl sulfoxide (DMSO), tetramethylene sulfone, dimethyl formamide, toluene etc.It is as follows to invent the described silsesquioxane structural formula that contains the aminophenyl cage modle.
(eight nitrophenyl cage-type silsesquioxanes) (eight aminophenyl cage-type silsesquioxanes)
Adopt eight aminophenyl cage-type silsesquioxanes of the inventive method preparation, utilize its amino reactivity worth, can prepare various matrix materials with Resins, epoxy, resol, oxazoline resin, oxazine resin, cyanate ester resin, bismaleimide resin, isocyanate resin etc., with resistance toheat, flame retardant properties and the mechanical property of improving resin.
Embodiment
Reduction efficiency: according to the H-NMR spectrogram, the integral area ratio value of the hydrogen of the phenyl ring hydrogen of oil of mirbane, the phenyl ring hydrogen of amino-benzene, amino obtains.
Embodiment 1: 1.79 mmoles (2.5 gram), eight nitrophenyl cage-type silsesquioxanes (hereinafter to be referred as ONPS), 50mL tetrahydrofuran (THF), Fe/C supported catalyst 2 grams are added in the 500mL there-necked flask, mix, be warming up to 60 ℃; Add hydrazine hydrate (80%), hydrazine hydrate and ONPS weight ratio are 3: 1, react stopped reaction again 4 hours.Reduce to room temperature, filter, add ethyl acetate extraction, in sherwood oil, precipitate, through separating, obtaining white precipitate after the drying, i.e. eight aminophenyl cage-type silsesquioxanes, productive rate 82%, reduction efficiency 100%.
Embodiment 2: with the method preparation eight poly-aminophenyl cage-type silsesquioxanes of embodiment 1, operation steps is identical with example 1, difference is that the weight ratio of hydrazine hydrate and ONPS is 2: 1, solvent is 1,4-dioxane, temperature of reaction are 100 ℃, finally obtain eight aminophenyl cage-type silsesquioxanes, productive rate 77%, reduction efficiency 100%.
Embodiment 3: the method with embodiment 1 prepares eight aminophenyl cage-type silsesquioxanes, operation steps is identical with example 1, difference is that eight nitrophenyl cage-type silsesquioxanes, solvent, Fe/C catalyzer three's weight ratio is 10: 200: 10, the weight ratio of hydrazine hydrate and ONPS is 8: 1, temperature of reaction is 50 ℃, finally obtain eight aminophenyl cage-type silsesquioxanes, productive rate 71%, reduction efficiency 99%.
Embodiment 4: the method with embodiment 1 prepares eight aminophenyl cage-type silsesquioxanes, operation steps is identical with example 1, difference is to use hydrazine hydrate (50%), and the weight ratio of hydrazine hydrate and ONPS is 8: 1, reacted 10 hours, finally obtain eight aminophenyl cage-type silsesquioxanes, productive rate 72%, reduction efficiency 98%.
Embodiment 5: the method with embodiment 1 prepares eight aminophenyl cage-type silsesquioxanes, operation steps is identical with example 1, difference is to use hydrazine hydrate (100%), and the weight ratio of hydrazine hydrate and ONPS is 2.5: 1, reacted 3 hours, obtain eight aminophenyl cage-type silsesquioxanes, productive rate 71%, reduction efficiency 100%.
Embodiment 6: the method with embodiment 1 prepares eight aminophenyl cage-type silsesquioxanes; operation steps is identical with example 1; difference is that reaction process reinforced, that drip reductive agent, continuation reaction is all carried out under nitrogen protection; finally obtain eight aminophenyl cage-type silsesquioxanes; productive rate 83%, reduction efficiency 100%.
Embodiment 7: the method with embodiment 1 prepares eight aminophenyl cage-type silsesquioxanes, operation steps is identical with example 1, difference is that eight nitrophenyl cage-type silsesquioxanes, solvent, Fe/C catalyzer three's weight ratio is 10: 50: 2, uses phenylhydrazine to be reductive agent, and the weight ratio of phenylhydrazine and ONPS is 8: 1, solvent is a toluene, reaction times is 6 hours, and temperature is 80 ℃, finally obtains eight aminophenyl cage-type silsesquioxanes, productive rate 62%, reduction efficiency 91%.
Embodiment 8: the method with embodiment 1 prepares eight aminophenyl silsesquioxanes; operation steps is identical with example 1; it is reductive agent that difference is to use phenylhydrazine, and the weight ratio of phenylhydrazine and ONPS is 8: 1, and solvent is a toluene; under nitrogen protection, react; reaction times is 11 hours, and temperature is 80 ℃, finally obtains eight aminophenyl cage-type silsesquioxanes; productive rate 73%, reduction efficiency 100%.
Claims (3)
1. the preparation method of an aminophenyl cage-type silsesquioxane is characterized in that, may further comprise the steps:
1) is that 10: 50～200: 2～10 eight nitrophenyl cage-type silsesquioxanes, solvent and Fe/C catalyzer stir in air or nitrogen atmosphere with weight ratio, is warming up to 50～100 ℃;
2) weight ratio according to eight nitrophenyl cage-type silsesquioxanes and reductive agent is 1: 2～8 adding hydrazine hydrate or phenylhydrazine reductive agents, reacts 2～12 hours;
3) reduce to room temperature after the reaction, filter, add ethyl acetate extraction, standing demix;
4) get organic phase behind the standing demix, in sherwood oil, precipitate, through separating, obtaining white precipitate after the drying, i.e. eight aminophenyl silsesquioxanes.
2. the preparation method of eight aminophenyl cage-type silsesquioxanes according to claim 1 is characterized in that, reductive agent is that mass concentration is 50～100% hydrazine hydrate or phenylhydrazine.
3, the preparation method of eight aminophenyl cage-type silsesquioxanes according to claim 1 is characterized in that, described solvent is ether, sulfone, acid amides and aromatic compound aromatics.
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| Application Number | Priority Date | Filing Date | Title |
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| CNB2006100808714A CN100412077C (en) | 2006-05-19 | 2006-05-19 | Process for preparing amino phenyl silsesquioxane |
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| CNB2006100808714A CN100412077C (en) | 2006-05-19 | 2006-05-19 | Process for preparing amino phenyl silsesquioxane |
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Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100430406C (en) * | 2006-09-21 | 2008-11-05 | 北京理工大学 | Method for preparing octamido phenyl silsesquixanes |
| CN100471898C (en) * | 2007-02-09 | 2009-03-25 | 南京大学 | Method of preparing star-type multi-arm silicon oil |
| CN101117441B (en) * | 2007-04-20 | 2010-06-02 | 北京化工大学 | Polyethylene silicon resin containing ethenyl cage model sesquialter siloxane and method for making same |
| CN1944441B (en) * | 2006-10-30 | 2012-01-25 | 北京化工大学 | Sesqui-siloxane containing benzoxazinyl group and its composition and preparing method |
| CN102391303A (en) * | 2011-10-24 | 2012-03-28 | 北京理工大学 | Preparation method of cage-type oligomeric octa(aminophenyl) polyhedral silsesquioxane (OAPS) |
| CN101372534B (en) * | 2007-08-24 | 2012-04-11 | 东丽纤维研究所（中国）有限公司 | Low dielectric coefficient polyimide/oligomeric silsesquioxane nano hybrid film and preparation thereof |
| CN102643304A (en) * | 2012-03-30 | 2012-08-22 | 山东大学 | Preparation method of cage poly (phenylsilsequioxane) |
| CN104292461A (en) * | 2014-09-16 | 2015-01-21 | 哈尔滨工业大学 | Preparation method of POSS modified PBO polymer |
| CN106188127A (en) * | 2016-07-11 | 2016-12-07 | 北京理工大学 | A kind of preparation method of ring trapezoidal nitrobenzophenone silsesquioxane |
| CN110467730A (en) * | 2019-09-10 | 2019-11-19 | 哈尔滨工业大学 | A kind of synthetic method of eight chloropropyls POSS |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002076438A2 (en) * | 2001-03-23 | 2002-10-03 | Chugai Seiyaku Kabushiki Kaisha | Flt-1 ligands and their uses in the treatment of diseases regulatable by angiogenesis |
-
2006
- 2006-05-19 CN CNB2006100808714A patent/CN100412077C/en not_active Expired - Fee Related
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100430406C (en) * | 2006-09-21 | 2008-11-05 | 北京理工大学 | Method for preparing octamido phenyl silsesquixanes |
| CN1944441B (en) * | 2006-10-30 | 2012-01-25 | 北京化工大学 | Sesqui-siloxane containing benzoxazinyl group and its composition and preparing method |
| CN100471898C (en) * | 2007-02-09 | 2009-03-25 | 南京大学 | Method of preparing star-type multi-arm silicon oil |
| CN101117441B (en) * | 2007-04-20 | 2010-06-02 | 北京化工大学 | Polyethylene silicon resin containing ethenyl cage model sesquialter siloxane and method for making same |
| CN101372534B (en) * | 2007-08-24 | 2012-04-11 | 东丽纤维研究所（中国）有限公司 | Low dielectric coefficient polyimide/oligomeric silsesquioxane nano hybrid film and preparation thereof |
| CN102391303A (en) * | 2011-10-24 | 2012-03-28 | 北京理工大学 | Preparation method of cage-type oligomeric octa(aminophenyl) polyhedral silsesquioxane (OAPS) |
| CN102643304A (en) * | 2012-03-30 | 2012-08-22 | 山东大学 | Preparation method of cage poly (phenylsilsequioxane) |
| CN102643304B (en) * | 2012-03-30 | 2015-07-29 | 山东大学 | A kind of preparation method of cage modle phenyl sesquisiloxane |
| CN104292461A (en) * | 2014-09-16 | 2015-01-21 | 哈尔滨工业大学 | Preparation method of POSS modified PBO polymer |
| CN106188127A (en) * | 2016-07-11 | 2016-12-07 | 北京理工大学 | A kind of preparation method of ring trapezoidal nitrobenzophenone silsesquioxane |
| CN106188127B (en) * | 2016-07-11 | 2020-04-07 | 北京理工大学 | Preparation method of ring-trapezoid nitrophenyl silsesquioxane |
| CN110467730A (en) * | 2019-09-10 | 2019-11-19 | 哈尔滨工业大学 | A kind of synthetic method of eight chloropropyls POSS |
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| CN100412077C (en) | 2008-08-20 |
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Granted publication date: 20080820 Termination date: 20170519 |