Reaction of 3-aminopropyltriethoxysilane with triphenylphosphate Текст научной статьи по специальности «Химические науки»

DOI: 10.14529/chem150409

REACTION OF 3-AMINOPROPYLTRIETHOXYSILANE WITH TRIPHENYLPHOSPHATE

V.V. Semenov, [email protected]

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, Nizhny Novgorod, Russian Federation

Interaction of 3-aminopropyltriethoxysilane RNH2 [R = (EtO)3SiCH2CH2CH2] with tri-phenylphosphate (PhO)3P=O proceeds at temperature 180-200 °C and leads to formation of quaternary ammonium salt of phenylphosphoric acid [PhOP(O)O2]2-[PhH2NR]2+, which turns into liquid silicon-containing oligoamidophosphates RNH[P(O)(OPh)NR]nP(O)(OPh)NHR and phenol at high temperature. The latter transesterifies the original 3-aminopropyltriethoxysilane and the obtained products. With the use of high-temperature vacuum rectification liquid oligomers and the solid cross-linked polymer have been isolated. Heating of the solid polymer up to 1000 °C in inert atmosphere results in the amorphous phase, containing SiO2 and NPO. The reactions of 3-aminopropyltriethoxysilane with triphe-nylphosphate and trimethylphosphate have been compared.

Keywords: 3-aminopropyltriethoxysilane, triphenylphosphate, trimethylphosphate, oligomers, thermal transformations.

Introduction

Molecules of triethoxysilylpropylamidophosphates (EtO)3SiCH2CH2CH2NRP(O)X2 (R = H, All; X = OR, NR2) contain the easily hydrolyzed group (EtO)3Si and the amidophosphate fragment NRP(O)X2, which can form coordination compounds with d- and f-elements. Ability of sol-gel polymerization and forming coordination compounds offers a way to obtain metal-containing gels, films [1], transparent glasses [2] on their basis. Target syntheses of such compounds are based on the reaction of 3-aminoprolyltriethoxysilane (EtO)3SiCH2CH2CH2NH2 (APTES) with the derivatives of phosphorous oxychloride ClP(O)X2 (X = OPh, NR2). Organic bases (triethylamine, pyridine) are used as acceptors of the evolving hydrogen chloride. Voluminous precipitates of triethylamine or pyridine hydrochlorides, produced in this reaction, badly thicken the reaction mixtures and demand great amounts of solvents, which need to be carefully dewatered, as the initial compounds and the products are hydrolytically unstable. In this context finding a more convenient method of obtaining alkoxysilyl derivatives of amido-phosphates seems an urgent problem. The alternative way of synthesis involves the reaction of two industrial products: APTES and triorganophosphates (RO)3P=O, which can lead to substitution of RO groups at the phosphorus atom and production of alcohol. Nevertheless, in recently performed study [3] it has been shown that interaction of APTES with trimethylphosphate (Me0)3P=0 (TMP) leads to release of ethyl (not methyl) alcohol in the first stage and production of organophosphosilicates. Replacement of methyl groups in triorganophosphate by phenyl ones has led to cardinal change of the process direction, so that release of phenol and production of silicon-containing amidophosphate oligomers has been observed. In the present paper the results in investigating APTES interaction with triphenylphosphate (Ph0)3P=0 (TPP) are described, the comparison of the related reactions is carried out, and the explanation of possible causes for different behavior of two structurally similar compounds (PhO)3P=O and (MeO)3P=O is suggested.

Experimental

IR spectra were recorded on the Fourier-transform IR spectrometer "FSM-1201". Liquid and resinous substances were spread in a film between KBr plates. In order to record solid samples a mineral oil suspension was prepared. Both :H and 31P NMR spectra of the samples dissolved in CDCl3 were recorded on the "Bruker Avance DPX-200" spectrometer, operating frequency equaled 200 and 80 MHz for :H and 31P, respectively; internal standard for :H was Me4Si, for 31P it was 85 % H3PO4. X -ray phase analysis was performed on "DRON-3M" diffractomerter (CuKa-emission) with the graphite monochromator on the diffracted beam. Thermogravimetrical analysis was performed on the "Perkin Elmer Pyris 6

TGA" apparatus. Heating of the 50 mg sample was carried out at the rate 5 deg per min from 40 to 1000 °C in nitrogen atmosphere. Mass spectra were obtained on the chromato-mass spectrometer "Trace GC Ultra" with mass analyzer "Polaris Q" (capillary chromatographic column NR-5MS, 30 m x 0.25 mm, thickness of stationary phase film 0.25 ^.m; injector temperature 250 °C; helium as the carrier gas; flow rate 1.5 mL per min; programmed temperature rise from 40 to 250 °C; mass analyzer with the ion trap; energy of ionizing electrons 70 eV; temperature of ion source 300 °C; the range of detected masses 40-400). Total ion current chromatograms were recorded. The analyzed mixture was dissolved in CH2Cl2. The sample volume equaled 1 |jl. Interpretation of mass spectra was carried out with the use of NIST MS Search 20 database.

APTES (Slavgorod PA "Altaikhimprom") was rectified under vacuum in the column 1x50 cm, filled by nichrome wire coils. TPP was recrystallized from heated toluene before use.

APTES was analyzed on the gas chromatograph "Tsvet-530" in the stainless steel column 0.3x200 cm, filled by solid support Chromaton-N-AW-DMCS with 5 % liquid phase XC-2-1; thermal conductivity detector; helium as the carrier gas; temperature of the column thermostat 160 °C, temperature of the detector and vaporizer thermostat 220 °C. Content of isomeric 2-aminopropyltriethoxysilane equaled 1.2 %. To analyze liquid fractions, obtained after distillation of oligomers under vacuum, the column 0.3x200 cm was used, filled by solid support Chromaton-N-AW with 5 % liquid phase SE-30; thermal conductivity detector; helium as the carrier gas; temperature of the column thermostat 200 °C, temperature of the detector and vaporizer thermostat 250 °C.

Reaction of APTES with TPP. APTES and TPP in molar ratio 1:1, 2:1 or 3:1 (Table 1) were placed at room temperature into a round-bottom flask with a stirrer and a reflux condenser.

Table 1

The reaction products of APTES with TPP

№ Quantity APTES, g (х102 mol) Quantity TPP, g (x102 mol) Weight of the collected liquid fractions, g (mas. %) (b. p., 0.05 mm Hg) Weight of fixed residue, g (mas. %)

1 (50-100оС) 2 (100-180оС) 3 (180-250оС)

I 9.52 (4.30) 14.00 (4.30) 3.06 (13) 10.58 (45) 4.70 (20) 5.18 (24)

II 9.52 (4.30) 7.00 (2.15) 1.65 (10) 8.93 (54) 2.48 (15) 3.46 (21)

III 9.52 (4.30) 4.70 (1.45) 1.14 (8) 8.68 (61) 1.71 (12) 2.70 (19)

The reaction mixture was heated in an oil bath up to 200 °C, then it was constantly stirred at this temperature for 8-10 h. After TPP was melted at 40-50 °C, the mixture became homogeneous, it time its viscosity increased. On completion of the process the viscous yellow liquids were obtained. Color intensity and viscosity decreased with increasing APTES content. The obtained products were distilled under vacuum in glass ampoules with attached side outlets. The ampoules were slowly heated up to 300 °C at the pressure 0.05 torr in a cylinder furnace with controlled output, and were kept at these conditions for 2 h. The temperature was registered with the use of a thermometer placed in the furnace. In Table 1 the distillation temperature intervals for corresponding fractions are shown, as well as the masses calculated in proportion to the initial amounts of reactants. All collected liquids were transparent and practically colorless, except fraction I-3 of yellowish color. The first fraction was condensed in the trap, cooled by liquid nitrogen, two others were collected into the side outlet and then detached. At 250 °C the mixture of oligomers began foaming. On completion of distillation and cooling to room temperature the formed yellowish foams were easily broken with a glass rod, turning into powders, insoluble in water and organic solvents.

All liquid fractions were analyzed by gas-liquid chromatography and chromato-mass spectrometry. In consequence of high-boiling components of the second and, especially, the third fraction transition into the gas phase and separation in the chromatographic column were hampered. The greater part of oligomeric products were not recorded by the given methods. In mass spectra phenol, APTES and several isomeric products, containing fragments of silicon alkoxides NHCH2CH2CH2Si(OEt)x(OPh)3_x, were determined unambiguously. Those compounds were contained in all distilled liquids, but the ratio was different. The first fraction included phenol with no more than 5 % admixtures of APTES derivatives. It was also demonstrated by IR spectroscopy data and the fact that the liquid, collected in the trap, har-

dened at room temperature (phenol m.p. 41 °C). The second fraction contained scarcely any phenol, while the third one was again enriched by phenol due to decomposition of the solid product.

Thermal decomposition of the solid product of APTES-TPP reaction. The weighed sample 1.01.5 g of the powder was placed in an ampoule, connected with a pump through a trap, kept under vacuum for 30 min and heated for 4 h at 400-420 °C. At that temperature the powder color changed from yellow to dark brown. In the side outlet, cooled by liquid nitrogen, gaseous products of pyrolysis were collected. The walls of the trap and the cold part of the apparatus were covered by white deposit. After cooling to room temperature the ampoule outlet was detached, the darkened powder was weighed. The loss of mass equaled 30-35 %. The gaseous decomposition products were refrozen through a connector under vacuum into an ampoule with a silicone stopper for chromato-mass spectrometry analysis. Those gases, representing not less than 70 % from the mass loss in the given stage, were the mixture of isomeric unsaturated hydrocarbons C3-C6. The white deposit from the outlet walls was dissolved in methylene chloride and also analyzed with the use of chromato-mass spectrometer. It consisted of phenol c 10 % admixture of elemental phosphorus P4.

After thermal treatment of the powder under vacuum the subsequent heating was carried out under nitrogen flow. The weighed samples 0.1-0.2 g of the powder obtained in the previous stage were placed in quartz boats 7x100 mm into a wide horizontal quartz tube, and nitrogen was blown through it for 1 h. Then they were heated in electric furnace at 600, 800, and 1000 °C, were allowed to stand for 5 h and cooled to room temperature. At 600 and 800 °C black powders were obtained, the loss of mass in those stages equaled not more than 5 %. Pyrolysis at 1000 °C led to formation of greyish sintered samples, the mass decreased by 40-50 %. In all those cases at the beginning of heating yellow-brown vapors were carried from the hot zone, with increasing temperature they carbonized.

In a similar way heating was carried out for the powder, obtained in the reaction of APTES with TPP, under oxygen flow at 1000 °C. The loss of mass equaled 45 %, practically colorless sintered material with greyish inclusions was obtained.

Results and Discussion

The reaction of APTES with TPP proceeds slowly only at heating up to 180-200 °C. Excess of APTES and short-term (3 h) heating at 150 °C does not result in interaction. In order to achieve higher conversion degree, it is necessary to heat at 180-200 0C during 10 h. The reaction mixture looks like a low-viscous liquid of pale yellow color. Phenol and ethyl alcohol have been found among low-boiling products by gas-liquid chromatography and IR spectroscopy.

Fig. 1 (curve 1) shows the IR spectrum of the products obtained after evaporation of alcohol and phenol under vacuum. The characteristic feature of the spectrum is the wide absorption band of high intensity, in the range from 3070 to 2200 cm-1, consisting of stretching vibrations of N-H bond in cation PhH2N-, together with superposition of less intensive absorption bands of stretching vibrations of C-H bonds of phenyl (3063, 3043 cm-1) and alkyl (2978, 2930, 2980 cm-1) groups. Deformation vibrations of N-H are represented as the shoulder 1620 cm-1. Presence of phenoxy groups (PhOP, PhOSi) is proved by the series of intensive bands caused by stretching (1595, 1493 cm-1) and out-of-plane deformation (691 cm-1) vibrations of the bonds C=C and C-H (shoulder 810 cm-1 and band 759 cm-1 of the doublet 759, 772 cm-1) [4]. The groups SiOEt are characterized by the series of bands 1161, 1094, 961 h 772 cm-1 [5]. The doublet 1246, 1212 cm-1 is related to vibrations of C-O and P-O bonds, respectively [6]. Widening of the band v(C-O) is caused by the simultaneous presence of groups POPh, SiOPh, SiOEt. Two bands of medium intensity 1452 and 1392 cm-1 are related to deformation vibrations of C-H bonds in -CH2- and -CH3 groups.

The IR spectroscopy data attest the presence in the reaction mixture of amine phenylphosphate salts Ia,b; which are formed through transfer of one or two phenyl groups from TPP to APTES nitrogen atom. Trie-thoxysilyl groups of these compounds are transetherifized by phenol, produced in the reaction (Scheme 1, reaction 5). Diamine phenylphosphate salt Ib can be obtained both at the interaction of Ia with APTES (Scheme 1, reaction 2) and as the result of Ia disproportionation (reaction 3), which is specific to organo-phosphoric acids (RO)2P(O)OH and their derivatives [7]. Phenol evolving suggests that Ia, b transform into phenyldiamidophosphate II, which then condenses into oligomeric amidophosphates III. Their identification becomes possible after distillation of the reaction mixture under vacuum at maximum underpressure and at temperature as high as 300 °C. At that amine salts Ia,b move into the vapor phase and are distilled only in a

minimal amount, which is attested by the IR spectroscopy data (Fig. 1, curves 3, 4). High temperature promotes reactions 4-6 and distillation of oligomers III. By and large their chemical nature is identical to 3-triethoxysilylpropylamidophosphate (EtO)3SiCH2CH2CH2NHP(O)(OPh)2 (IV), that we have synthesized earlier [1].

4000 3000 2000 1000 v, cm"1

Fig. 1. FTIR spectra of the reaction products of equimolar quantities of APTES with TPP: 1 - a reaction mixture after removal of a great bulk of ethanol and phenol; 2 - fraction I-1; 3— fraction I-2, 4 - fraction I-3 (liquid films)

(Ph0)3P=0 HqNR

IIoNR

[(Ph0)2P(0)0]"[PhH2NR]+ la

la

2 la ^

200 °C „

[Ph0P(0)02] [PhH2NR]2 lb

lb + (Ph0)3P=0

lb

PhOP(O) (NHR)2 + 2 PhOH II

-Si(OEt)3 PhQH> -Si(OEt)x(OPh)3.

nil

-EtOH 200 °C

(1) (2)

(3)

(4)

(5)

V RNH[P(0)(0Ph)NR]nP(0)(0Ph)(NHR) + 1/n RNH2 (6) III

R = CH2CH2CH2Si(OEt)x(OPh)3.x

Scheme 1

Fig. 1 represents IR spectra of three fractions separated in the result of distillation of the reaction mixture APTES : TPP = 1 : 1. The first fraction (curve 2) constitutes the mixture of phenol with APTES. In two high-boiling fractions (curves 3 and 4) accumulation of PhO groups takes place, at that they are bonded not only to the phosphorus atom, but also to the silicon atom. The consequence is the intensity decrease of the most characteristic band (1083-1103 cm-1) of Si(OEt)3 fragment vibrations in relation to the stretching vibration band of C-O bonds (1246 cm-1).

The intensity of bands v(C-H) of phenoxy radicals (3066, 3040 cm-1) in relation to v(C-H) of aliphatic radicals increases significantly. The most high-boiling fraction contains the greater part of the product completely transetherifized by phenol and the unreacted TPP. The character of the spectrum in the range 3500-3100 cm-1 attests that the band v(N-H) in oligomers is of low intensity. The observed wide band of medium intensity at 3300 cm-1 corresponds to stretching vibrations of the phenol hydroxyl group, which is admixed to all the fractions.

The possibility of transetherification has been examined by the example of phenol reaction with APTES. Heating of their equimolar mixture at 180-190 °C for 3 h has led to consumption of initial reac-tants and to formation of one main high-boiling compound (according to gas-liquid chromatography data), which constitutes 3-aminopropyldiethoxyphenoxysilane.

Thus, the reactions represented in scheme 1 include not only the initial APTES, but also its transetherifized derivatives. Their formation is most probable when reaction proceeds with an excess of APTES.

The 1H NMR spectroscopy data also suggest increasing the content of phenoxy radicals in high-boiling oligomers obtained by high-temperature vacuum rectification. Comparison of the :H NMR spectra for the reaction mixture APTES : TPP = 2 : 1 before distillation, as well as the second and third fractions, to the spectrum of the model compound amidophosphate IV, shows the following results. In the amidophosphate IV spectrum there are three groups of lines with equal intensity: 0.47-0.55, 1.49-1.56, 2.97-3.03 ppm, that characterize three methylene fragments between the atoms of silicon and nitrogen SiCH2CH2CH2N. Ethoxy substituents are represented by the intensive triplet at 1.12 ppm (CH3) and the quadruplet 3.74 ppm (CH2). The proton resonance of phenoxy groups at the phosphorus atom appears as the multiplet in the range 7.08-7.25 ppm. Formation of SiOPh fragments in the reaction mixture leads to significant complication of the :H NMR spectrum. First of all, two new multiplets appear, which are positioned to the right of the similar group of lines belonging to the PhOP fragment. The triplet of the methyl fragment and the quadruplet of the methylene fragment of ethoxy groups transform into multiplets owing to appearance of the mixed (ethoxy)(phenoxy)silyl groups Si(OEt)x(OPh)3-x. Three groups of lines of the fragment SiCH2CH2CH2N in compound I are supplemented by the multiplet 0.97-1.07 ppm, which is related to the methylene fragment -CH2-Si(OEt)x(OPh)3-x (influence of electron-accepting PhO groups, transmitted by the silicon atom). In the spectra of distilled fractions these differences are strengthened. Even greater increase of the proton resonance intensity for phenyl groups, bonded to the silicon atom, takes place, and proportional decrease of intensity for bands related to ethoxysilyl substituents. In the most high-boiling fraction the content of SiOEt groups becomes minimal, which follows from very low intensity of signals at 1.1-1.3 ppm. Appearance of two resonances at 5.47 and 5.55 ppm is observed in the second fraction, they are probably related to the hydrogen atoms of the terminal amidophosphate groups -P(O)-NH-. They are not located in the third the most high-boiling fraction. According to scheme 1, in the reaction mixture without rectification quaternary ammonium base PhH2N-CH2CH2CH2-Si(OR)3 should be present. It is known [8] that the resonances of the methylene fragment N-CH2 in the compounds of such kind are located near 3.7 ppm, that is, they are superimposed by the signals of SiOCH2 group. Indirect confirmation of amine salt existence follows from the intensive widening and splitting of the multiplet band related to the central methylene group. The new band with the center at 1.77 ppm appears because of electron-accepting influence of the group PhH2N-CH2-. In the second fraction quaternary amine salt is practically absent, and the proton resonances of the central methylene fragment appear as one widened band with the center at 1.68 ppm. In the third fraction accumulation of electronegative groups Si(OPh)3 [compared to Si(OEt)3] once again leads to widening and splitting of this band. Overintensity of the multiplet 2.5-2.8 ppm, belonging to the fragment -CH2-N, engages our attention. Presumably other organic amines, besides the silicon-containing one, are present in the mixture; they are produced as the result of its high-temperature treatment both during the synthesis process itself and during its rectification.

The changes of :H NMR spectrum for the reaction mixture APTES : TPP = 1 : 1 and the fractions isolated from it are similar to the above, as a whole. The 1H and 31P NMR spectroscopy data demonstrate that the greater part of TPP remains unreacted, whereas APTES is consumed comparatively fast and to the fullest extent. The presence of unreacted TPP attests that reactions 1-4 (scheme 1), leading to compounds Ib and II with the ratio Si : P = 2 : 1, proceed easier than the following condensation and formation of oligomers III (reaction 6), in which the ratio Si : P approaches one. The transetherification of trie-thoxysilyl groups by phenol proceeds with efficiency, the appearance of ethylphosphate fragments can be observed. In the spectra of 2- and 3-fractions there are the signals of the group CH3-CH2-OP(O) protons at 1.3 ppm (multiplet) and 4.3 ppm (triplet).

The differences in the :H NMR spectra changes for the products of the APTES-TPP reaction, carried out at the ratio 3:1, are determined by the greater rate of phenol consumption for the use in transetherification of APTES that is in excess. The formed phenoxylated organosilicon amines are of less reactivity concerning TPP. Because of this in excess conditions the initial APTES reacts first of all, while the evolving phenol is expelled from the process mostly in the form of phenoxylated APTES derivative. Thus, the rate of oligoamidophosphate phenoxylation decreases, if there is an excess of organosilicon amine in the reaction.

Association of phenol with amidophosphate groups does not allow to separate it by rectification completely. Effective decrease of its concentration in oligomers is reached by treatment of APTES-TPP reaction products by hexamethyldisilazane at heating. Ammonia evolves intensively and phenoxytrime-thylsilane forms, which has been isolated, purified by rectification and identified by gas-liquid chromatography and IR spectroscopy [9].

Additional information about the composition of the liquid products is provided by 31P NMR spectroscopy data. Table 2 presents the relative intensity of the signals for oligomers before distillation and in two high-boiling fractions. The signal S = -10 ppm is contained in the spectra of all the products. In the spectra of distilled fractions the second signal appears S = -11 ppm. It is also present in the spectrum of the product of APTES : TPP = 1:1 before distillation.

Table 2

Relative intensity of signals in 31P NMR spectra of oligomers obtained in reaction APTES with TPP

Oligomers Re ative intensity of signals

S = -10 ppm S = -11ppm S = -16.5 ppm

Before destination 1.0 0.1 0.03

I Fraction I-2 1.0 0.8 0.6

Fraction I-3 1.0 1.9 0.3

Before distillation 1.0 - -

II Fraction II-2 1.0 0.5 -

Fraction II-3 1.0 0.7 -

Before destination 1.0 - -

III Fraction III-2 1.0 0.1 -

Fraction III-3 1.0 0.2 -

Only in the latter and in two fractions obtained from it the signal S = -16.5 ppm is observed, it is related to the unreacted TPP. The relative intensity of the signal S = -11 ppm is maximal at the ratio APTES : TPP = 1:1, it decreases with increasing APTES content. Furthermore, its contribution is always greater in the most high-boiling fraction. On the basis of qualitative patterns concerning correlation between the chemical shifts of 31P nuclei and the nature of substituents in various phosphorus-nitrogen compounds [10, 11], the signal S = -10 ppm can be correlated with the phosphorus atoms in -NHP(O)(OPh)- groups, which the signal S = -11 ppm with those in -NRP(O)(OPh)- groups.

The data presented in Table 2 involve the following conclusions.

When the reaction is carried out at ratio 1:1, not all TPP reacts. The APTES excess leads to its complete consumption.

In the process of high-temperature vacuum rectification oligomers with formula III (Scheme 1) are accumulated. Their content decreases at dilution of the initial mixture by 3-aminopropyltriethoxysilane. The latter circumstance is connected to the lower phenoxylation degree of oligomers, and, consequently, to the significantly lower temperatures necessary for completion of rectification process. If organosili-

con amine is in excess, the evolving phenol is largely consumed for the APTES phenoxylation, during rectification process it is distilled in the form of its derivatives. The formed amidophosphate oligomers contain smaller amount of Si(OEt)x(OPh)3-x groups. As a consequence, in the process of vacuum rectification they move into the vapor phase and are distilled away at relatively low temperature (under 250 °C), which is nevertheless sufficient to start the condensation process described by equation 6 in Scheme 1. High temperatures (up to 300 °C) are necessary to distil maximally phenoxylated oligomers that are produced in the reaction of APTES : TPP = 1:1. In this connection they contain greater amount of condensed oligomers, that is also expressed in their greater viscosity.

In addition to three main signals (-10, -11, -16.5 ppm) in the 31P NMR spectra of the isolated fractions there is a series of low-intensive signals, attesting to complication of the mixture composition during the process of high-temperature rectification ((250-300 °C / 0.05 torr). The formed admixtures are not recorded in the original products before distillation. The complication of the composition during the rectification process is observed to a lesser extent for the products of the reaction with reactant ratio 2:1; it is absent for the products of the process with the reactant ratio 3:1. The observed pattern is connected to decreasing temperature during rectification of the products for the reactions, carried out with an excess of APTES. The low-intensive signals, recorded by 31P NMR method, are related to the mixed structures, in which fragments -[OP(O)(OPh)O]-, -[OP(O)(OPh)NR]-, -[OP(O)(OPh)NH]-, and -[OP(O)(OPh)OSi(OR)2]- alternate.

After the liquid products have been distilled away under vacuum, at the temperature increasing up to 300 °C the yellow-brown foam is left in the apparatus; it is easily broken with a glass rod into a powder that is insoluble in water and organic solvents. The mass of the powder equals up to 24 % of the mass of the reaction mixture taken for distillation. The nature of the solid product of the APTES-TPP reaction has been established by thermogravimetric analysis, IR spectroscopy, chromato-mass spectro-metry, X-ray phase analysis, and elemental analysis.

Fig. 2 presents the thermogravimetric curves of the obtained powder. The main loss of mass takes place in the temperature range 400-450 °C. The products of thermal decomposition, according to chro-mato-mass spectrometry data, are the mixture of gaseous unsaturated hydrocarbons C3-C6, phenol and elemental phosphorus. Hydrocarbons form as the result of decomposition of the fragments NCH2CH2CH2Si. Phenol evolves at condensation of phenylphosphate and amidophosphate groups.

O O

-P-OPh + H^-

O

II

P-N-P-

PhOH

+

Phosphorus is the product of high-temperature reduction of amidophosphate derivatives by carbon components [12]. The next stage of the mass loss at temperature higher than 450 °C is related to increasing reduction efficiency of the phosphorus derivatives and removing it in the form of P4, possibly also as NPO [13]. Besides thermogravimetric analysis the powder has been thermally treated in stages at 400, 600, 800, and 1000 °C in an argon atmosphere, in order to establish the nature of the thermal decomposition products. The powder color have changed from yellow to dark brown (400 °C), black (600 and 800 °C), and grayish white (1000 °C). Transition from the intermediate black (caused by amorphous carbon) to the final pale color of the pyrolysis products (SiO2 and NPO) is in accordance with the reduction of phosphates by carbon, known from the literature [12]. All ignited samples are amorphous. The change of IR spectra at thermal transformation, shown in Fig. 3, fits the processes described above.

In the IR spectrum of the original product (Fig. 3, curve 1) the bands of phenyl groups are observed: stretching vibrations C-H (shoulder at 3070 cm-1), planar stretching vibrations (1594, 1489 cm-1) and out-of-plane deformation vibrations of the bonds C=C (690 cm-1) and C-H (768 cm-1). Likewise, the spectrum includes the bands of stretching vibrations (wide absorption 3500-3200 cm-1) and deformation vibrations (1628 cm-1) of the bond N-H. In the range 1250-900 cm-1 badly defined bands are concentrated, they correspond to the fragments P(O)N (1212 cm-1) and SiOR (1073, 1026, 921 cm-1). In the IR spectra of all heated samples absorption of PhO and EtO groups is absent. With increasing temperature the intensity of the bands related to vibrations of the bond N-H decreases.

m (%); dm/dT

Fig. 2. Integral (1) and differential (2) curves of the solid product of reaction APTES with TPP

4000 3000 2000 1000

Fig. 3. Transformation of FTIR spectrum of the solid product of reaction APTES with TPP on heating: 1 - the initial sample, 2 - 400 °C, 3 - 600 °C, 4 - 800 °C, 5 - 1000 °C (suspensions in Nujol)

The IR spectrum of the sample, thermally treated at 1000 °C in argon, matches the superposition of the amorphous SiO2 and NPO spectra (Fig. 3, curve 5). Even at 400 °C the well-defined, though low-intensive, band of symmetrical stretching vibrations of the fragment SiOSi appears at 800 cm-1. Its intensity sharply increases after thermal treatment at 1000 °C. The band of symmetrical stretching vibra-

tions of SiOSi at 465 cm-1 appears also at 400 °C. It is widened and highly intensive. Heating at 1000 °C causes decrease in width and further increase in intensity.

The IR spectrum of amorphous silica, according to data [14, 15], includes 6 absorption bands: deformation vibrations of the absorbed water H-O-H 1635 cm-1; stretching vibrations of the bond Si-O in Si-OH groups 1214 cm-1; LO-mode of asymmetrical stretching vibrations of the fragment Si-O-Si 1100 cm-1; TO-mode of asymmetrical stretching vibrations of the fragment Si-O-Si 970 cm-1; symmetrical stretching vibrations of Si-O-Si 805 cm-1; symmetrical deformation vibrations Si-O-Si 470 cm-1. The band 1100 cm-1 is the most intensive. All the bands except 1214 cm-1 are usually well-defined.

It is known [16] that in the IR spectrum of amorphous phosphorus oxynitride three wide absorption bands are present: at 1500 - 1250, 1150 - 900, and 450 - 550 cm-1 with centers at 1350, 1000, and 1500 cm-1.

The resultant spectrum (Fig. 3, curve 5) resembles the spectrum of amorphous silica to a great extent. The differences, that are explained by the presence of the amorphous phase NPO, are expressed in widening of the most intensive band 1100 cm-1. The intensity of the band related to symmetrical deformation vibrations of SiOSi at 470 cm-1 is enlarged compared to pure silica, with the sacrifice of the respective band 450-550 cm-1, which is the most intensive in the spectrum of phosphorus oxynitride. Vibrations of the bond P=O are represented by absorption at 1337 cm-1. The final product (Fig. 3, curve 5) is weakly hydrated, which is corroborated by the low-intensive band of stretching vibrations of the bond O-H at 3442 cm-1. Markedly lower component of NPO compared to SiO2, registered by IR spectroscopy, is the consequence of significant loss of phosphorus at pyrolysis. The intermediate and final spectra, presented in Fig. 3, do not correlate to the spectra of phosphosilicates [17, 18], which could in principle have been produced at thermal decomposition of the solid product of the APTES-TPP reaction.

Annealing the solid product of the APTES-TPP reaction under oxygen flow, as expected, has led to formation of the mixture of crystal and amorphous phosphosilicates. X-ray phase analysis (Fig. 4) has shown that the annealed sample represents the mixture of three crystal modifications: hexagonal Si5O(PO4)6, monoclinic and cubical SiP2O7; it also includes noticeable amount of amorphized component.

5

25

45

29 (°)

Fig. 4. X-ray patterns of the reaction product of APTES with TPP thermally treated on 1000 °C

in argon (1) and in oxygen (2)

The elemental analysis data for the solid products of the APTES-TPP reaction, heated under vacuum at 300 °C, are shown in Table 3.

Table 3

The element analysis of solid residue from reaction APTES with TPP

Starting proportion of APTES:TPP Content of elements, mas. %

C H N P Si

1:1 24.43 4.24 4.37

2:1 23.56 5.21 4.00 15.24 12.59

3:1 23.29 5.43 4.12

It follows that the composition of the products changes but insignificantly with the ratio of initial reactants. It should be mentioned that in the powder obtained at the ratio APTES : TPP = 1:1 the content of carbon is somewhat greater, while the content of hydrogen is lower. The ratio Si : P is still 1:1, in spite of the fact that APTES has been taken in excess. Based upon the data of elemental and X-ray phase analysis, as well as the IR spectroscopy data, the obtained product can be described as the cross-linked polymer, containing structural fragments OP(O)N(CH2^Si(OEt)O, P(O)OO, Si(OEt^O, Si(OEt)(OPh)O to the ratio 1 : 0.6 : 0.5 : 0.1.

The factual findings are in agreement with the data in the literature [7, 19, 20] about thermal transformations of amidophosphates.

Thus, the interaction between APTES and TPP proceeds only at high temperature and leads to producing phenol, ethyl alcohol and liquid amodophosphate oligomers. Phenol is consumed in transetherifi-cation of triethoxysilyl groups to a large extent. In the process of high-temperature vacuum rectification of the oligomers the solid insoluble cross-linked polymer is formed, which is structurally more or less related to the liquid products. Thermal decomposition of the cross-linked polymer (400-1000 °C) in the inert atmosphere gives the amorphous mixture composed of silicon dioxide and phosphorus oxynitride.

The APTES-TPP reaction paths and the properties of the obtained products are cardinally different from the data found earlier by us [3], concerning the similar reaction between APTES and trimethyl-phosphate. The interaction of APTES with TMP and TPP begins with the transfer of organic radical (Me or Ph) from the group POR to the nitrogen atom of organosilicon amine and formation of the amine salt of dimethyl- or diphenylphosphoric acid, which disproportionates into the salt of methyl-(phenyl-)phosphoric acid. In the course of the APTES-TMP reaction the acid-base properties of the mixture change from basic (because of APTES) to neutral to acidic, which is explained by formation of free me-thylphosphoric acids (MeO^P(O)OH and MeOP(O)(OH)2. In the APTES-TPP reaction the basic medium, due to the presence of organosilicon amine, is still weakly basic to the end of the reaction. This indicated the absence of free phenylphosphoric acids (PhO)2P(O)OH and PhOP(O)(OH)2 in the reaction mixture. To summarize, the key point that distinguishes two similar processes (APTES-TMP and APTES-TPP) is the presence of free methylphosphoric acids in the first case and the absence of phenylphosphoric acids in the second case. Methylphosphoric acids interact with APTES and its methylated derivative according to the reaction path of substitution of OEt group at the silicon atom and the formation of methylphosphosiloxane, which easily polymerizes at medium (100-120 °C) temperature. Owing to the absence of free phenylphosphoric acids, the similar reaction with Si(OEt)3 group cannot be realized, as a consequence, the amine salt of phenylphosphoric acid transformation into diamidophosphate and phenol becomes preferential.

Scheme 2 shows the main directions of the APTES reactions with TMP and TPP (without going into detail).

Different nature of the obtained compounds predetermines their following thermal transformations. Polymethylphosphosiloxane, containing the structural fragments Si-O-P, produces crystalline phospho-silicates, which polyamidophosphate, containing the P-N groups, gives the mixture of amorphous SiO2 and NPO.

Previously in papers [21-23] it has been shown that the mixture of oligomers, obtained as the result of the APTES-TPP reaction, can be used in the capacity of fast-cured lacquer, forming colorless transparent photo- and heat-resistant coatings. The results of the present study make it possible to evaluate

the chemical composition of the coatings generated from organophosphorus-silicon oligomers after high-temperature treatment.

O f

(MeO)3P=O + NH2-► 1/n—|-P-O-Si-Oi^ + 2 EtOH + MeOH

; MeO

\ NHMe

Si(OEt)3

O

(PhO)3P=O + NH2-► 1/n—[-p—N-lr + 2 PhOH

> PhO >

Si(OEt)3 Si(OEt)3

Scheme 2

Acknowledgements

The research was supported by the Russian Academy of Sciences: Complex program of RAS Presidium "Directed synthesis of substances with required properties and preparation of functional materials on their basis". The study was carried out with the use of the equipment of the Analytic center in Razu-vaev Institute of Organometallic Chemistry, Russian Academy of Sciences.

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Received 10 September 2015

УДК 546.287+546.185+547.1-315 DOI: 10.14529/^ет150409

РЕАКЦИЯ 3-АМИНОПРОПИЛТРИЭТОКСИСИЛАНА С ТРИФЕНИЛФОСФАТОМ

В.В. Семенов

Институт металлоорганической химии им. Г.А. Разуваева РАН, Нижний Новгород

Взаимодействие 3-аминопропилтриэтоксисилана RNH2 ^ = (ЕЮ)^ЮН2СН2СН2] с трифенилфосфатом (PhO)зP=O протекает при температуре 180-200 °С и приводит к образованию четвертичной аминной соли фенилфосфорной кислоты ^0Р(0)02]2-[Р11Н2МЯ]2+, которая в условиях высокой температуры превращается в жидкие крем-

нийсодержащие олигоамидофосфаты RNH[P(O)(OPh)NR]nP(O)(OPh)NHR и фенол. Последний переэтерифицирует исходный 3 -аминопропилтриэтоксисилан и получающиеся продукты. Методом высокотемпературной вакуумной ректификации выделены жидкие олигомеры и сшитый твердый полимер. Нагревание твердого полимера до 1000 °С в инертной атмосфере дает аморфную фазу, состоящую из SiO2 и NPO. Проведено сравнение реакций 3-аминопропилтриэтоксисилана с трифенилфосфатом и с триметилфос-фатом.

Ключевые слова: 3-аминопропилтриэтоксисилан, трифенилфосфат, триметил-фосфат, олигомеры, термические превращения.

Литература

1. Спектрально-люминесцентные свойства кремнийорганических амидофосфатов и их комплексов с европием и эрбием в растворах и в пленках / В.В. Семенов, Н.Ф. Черепенникова, Л.Г. Клапшина и др. // Координационная химия. -2005. - Т. 31, № 7. - С. 550-558.

2. Синтез и оптические свойства наногибридов в системе кремнезем-триамидофосфатные комплексы лантаноидов / Н.Н. Химич, Ю.Л. Зуб, Л.А. Коптелова и др. // Журнал прикладной химии - 2006. - V. 79, № 11. - P. 1769-1774. DOI: 10.1134/S 1070427206110061

3. Синтез и термические превращения полифос-фосилоксана на основе триметилфосфата и 3-аминопропилтриэтоксисилана / С.В. Клементьева, Н.Ф. Черепенникова, В.В. Семенов и др. // Изв. АН. Серия химическая - 2007. - № 11. - С. 2138-2148.

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6. Атлас ИК-спектров фосфорорганических соединений: (интерпретированные спектрограммы) / Р.Р. Шагидуллин, А.В. Чернова, В.С. Виноградова, Ф.С. Мухаметов. - М.: Наука, 1984. - 334 с.

7. Нифантьев, Э.Е. Химия фосфорорганических соединений / Э.Е. Нифантьев. - М.: Изд-во МГУ, 1971. - 352 с.

8. Tables of Spectral Date for Structure Determination of Organic Compounds / E. Pretsch, Clerc Th., J. Seibl, W. Simon. - Berlin: Springer Verlag, 1989. - P. 75.

9. Wilson, G.R. Preparation, Properties and Infrared Spectra of 2,6-Disubstituted Phenoxysilanes / G.R. Wilson, A G. Smith, F.C. Ferris // J. Org. Chem. - 1959. - V. 24, № 11. - P. 1717.

10. Nielsen, M.L. Phosphorus - 31 nuclear magnetic resonance studies of phosphorus - nitrogen compounds / M.L. Nielsen, J.V. Pustinger // J. Phys. Chem. - 1964. - V. 68, № 1. - P. 152-158.

11. Самитов, Ю.В. Химия и применение фосфорорганических соединений. Труды третьей конференции / Ю.В. Самитов, Т.В. Зыкова. - М.: Наука, 1972. - С. 49-74.

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14. Shibata, N. Raman Spectra of Binary High-silica Glasses and Fibers Containing GeO2, P2O5 and B2O3 / N. Shibata, M. Horigudhi, T. Edahiro // Journal of Non-Crystalline Solids - 1981. - V. 45. № 1. - P. 115-126.

15. Bertoluzza, A. Raman and Infrared Spectra on Silica Gel Evolving Toward Glass / A. Bertoluz-za, C. Fagnano, M.A. Morelli, V. Gottardi, M. Guglielmi // Journal of Non-Crystalline Solids. - 1982. -V. 48. - № 1. - P. 117.

16. Миллер, Т.Н. Неорганические соединения фосфора с азотом / Т.Н. Миллер, А.А. Витола. - Рига: Зинатне, 1986. - 208 с.

17. Воронков, М.Г. Кремнекислородные соединения неметаллов. Производные азота и фосфора: монография / М.Г. Воронков. - Новосибирск: Наука, 1988. - 365 с.

18. Thermal Evolution of Sol-gel-obtained Phosphosilicate Solids (SiPO) / P. Massiot, M.A. Centeno, I. Carrizosa, J.A. Odriozola // J. Non-Cryst. Solids. - 2001. - V. 292, № 1-3. - P. 158-166.

19. Dishon, B. Trimeric phosphonitrillic dibutyl and dimethyl ester / B. Dishon // J. Am. Chem. Soc. - 1949. - V. 71, № 6. - P. 2251-2253.

20. Steger, E. Infrarotspektroskopische Untersuchungen zur Bildung von Phosphornitroxid aus Phosphorsauretriamid und zu seiner hydrolytischen Zersetzung / E. Steger, E. Mildner // Z. Anorg. Allgem. Chem. - 1964. - B. 332, № 5-6. - P. 314-316.

21. Пат. 2418024 Российская Федерация, МПК C09D 183/08, C08G 77/30. Быстроотверждае-мый термостойкий лак и способ его получения / В.В. Семенов, Е.Ю. Ладилина, Т.С. Любова; патентообладатель Учреждение Российской академии наук Институт металлоорганической химии им. Г.А. Разуваева РАН (RU). - № 2418024; заявл. 10.11.2009; опубл. 10.05.2011. - 14 с.

22. Семенов, В.В. Быстроотверждаемое термостойкое покрытие на основе фосфорсодержащего кремнийорганического лака / В.В. Семенов // Журнал прикладной химии. -2013. -Т. 86, № 11. - С. 1831-1836.

23. Семенов, В.В. Покрытия на основе фосфорсодержащего кремнийорганического лака и кремнийорганического периленового красителя / В.В. Семенов // Лакокрасочные материалы и их применение. - 2011. - № 8. - С. 34.

Семенов Владимир Викторович - доктор химических наук, зав. лабораторией кремнийор-ганических соединений, Институт металлоорганической химии им. Г.А. Разуваева РАН. 603950, г. Нижний Новгород, ГСП-445, ул. Тропинина, 49. E-mail: [email protected]

Поступила в редакцию 10 сентября 2015 г.

ОБРАЗЕЦ ЦИТИРОВАНИЯ

Semenov, V.V. Reaction of 3-aminopropyltriethoxysilane with triphenylphosphate / V.V. Semenov // Вестник ЮУрГУ. Серия «Химия». - 2015. - Т. 7, № 4. -С. 66-79. DOI: 10.14529/chem150409

FOR CITATION

Semenov V.V. Reaction of 3-Aminopropyl-triethoxysilane with Triphenylphosphate. Bulletin of the South Ural State University. Ser. Chemistry. 2015, vol. 7, no. 4, pp. 66-79. DOI: 10.14529/chem150409