SCIENTIFIC ABSTRACT M.F. CHEBUKOV - I.V. CHEBUSHEV

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SCIENTIFIC ABSTRACT
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ACC NRi AP7007510 souRcE com: Wbiol/67/boo/bbi/0012/0013 jAUTHOR: Chebukoy M F (Professor); Ignatlyevao L, P. (Candidate of itechnical sciences) 'ORO-. Ural Polytechnic Institute (Urallskly politekhnicheakly institut) .TITLE: Boric acid from ores ,SOURCE: Teement,, no, 1, 1967, 12-13 4*JV TOPIC TAGS: boron mineral, datolites gypsum i cement A16"MCT2 The Urals Scientific Research Chemical Institute has developed a method fii obtaining boric acid from datolite and loan borate ores from Far Eastern regions. The method'is based on.grLuding rocks and leaching then with sulfuric acid. Large mounts of gypsum are obtaimed as a by-pro- duct.- It to suggested that gypsum-r1ch by-products of the datoll-te processing be used at the Far Usters cement plaqts, as additives to clinkers instead ok M M'um Imported from the central regions of the cod 1A UDC t ACC Nit- AP7007510 USSR. These far Eastern cesient plaute can coisame up to 100.000 ton of gypsum yasrly (the infanotion Is of Interest because It IndLeat" the potentlal scale of"Astolite Xwk processed for borm compovMsl,. OrU art. has: I tsible. INC! DATU: non 5117 SUB CODEs OT4j-3UMK, e/ ATD PRMt 7,AviumV. V,, pApoUtuvnlkj CHMTAV-Vv reg Uwardii polpollcvrlk ze-pasa I~wjow md bjbljoCmft* Komm6 VooLw&o Bile 46 no* 23LI M-M 11 165 (IMA 1911) USSR/Diseases of Farm Ardnals. General Problems. Abs Jours Ref Zhur - Biol., No 1. 1959j, 2791 Author 'Chebunin, S. M. Inst k-as-01-VU-irtiary, Institute Title Clinical and Pathomorphological Chara- cteristics of Acute Experimental Myo- cardium lWairmentso Orig Pub: Uch. sap. Kazansk. vet. in-ta, 195~, 65, 57-68 Abstracts No abstract Card 1/1 R-1 CHEBUNIN, S. M. Cand Vet Sci -- (diss) "Acute affections of the myocardiu-m in animals.and their treatmeit with novocain blocl:o of the stellate~~glion region (Ob**Aot4 i~lperimental study)." Kazan', 1958. 17 pp (Min of Agr USSR C, Kazant State Vet Inst im N. E.. Bauman). (KL, 52-58, 105) -496- --CHMUNINA, A.K., uchitelluitea lAboratory work in botany. Siol.v shkole no.2-.92 Mr-Ap l6o. (MIR& 13:8) 1. Shkola ND. 313 goroda Moskvy. (Botamy-Study and teaching) HASHIp ANN11U#-AL4., whitellaitea Independent work of students stodying the higher nervous anima2se Dicle v shkole no.2:30-34 Mr-1p 161.' (=314T3 ') 1. Inatiftt Pbsbabigo i po2itakhnichaskogo obrasovaniya Akadmil, pedaga- gichaskm nauk Run Pror MW. 2. Okola NO.315 go. Koskn (for Chebu"). Physiology-Study and teachiig) iConditioned response) CHEBUNINA, A. N., -AP~h - System of students' independent work in botany, Riol. v sbkole no.3-:26-22 Ja-Y 163. MMA 16.-6) 1. Shkola No. 315, Moskva. (BotaM,--Study and teaching) GREBUNIKOVAS F. [translator); GALIFFROAt T. [translator] C-. In foreign coun"89 Niasind. 553R 33 [i.e.341 no.2:59-61 163. . (MIRA 16-4) (Heat industry-Equipment and-supplies) ,I - :, ;-I -, polkovnik zapasa ,q; 1-1 ~- - . - ~ ~ -.- -, -- of elders. Komm. Vooruzh. Sil 4 no.108-60 Jlj 164. (MIRA 170) 1. Chlen Soveta veteranov kommnisticheskogo Soyuz~i nolode-hi. CHIBMAIHIN, Aleksancir Tey",yevich- GRMKIY, Genrlkh RafailovIch; TATAUNKO. W SNIMMUMOV, S., r0laktor; ITANOT. K.A.. redmktor 9 Isdotelletva; TIZHCKOFA, Ye.A., tekhnIcheekly redaktor [work practice of the dredge OBudsuarig of the ALoy Adminstration of Seaways] Opyt raboty ekipasha semanarlads wDadennyiO asovskogo upravlantla norskikh putel. Moskva, Isa-vo ONorskol transport.* 1956e 51 P. (NIU 9:12) (Drafting) CHIBURAMIIX,-AlokmLudr~lweepwich.--AGASHIN. N.I. red.; ZINOVqZU,A.A., red. ids-va.; LAVRIZOVA. N.B., tekhz6 red*' (Practices of maintenance men In the navigational aid service In the Sma of Azov] Q~jt raboty puisitsey Asovtla. Hookwa Ind-vo mKordbol transport 1957. 44 p. IKIRL 1117) Urt- Sea of-Aide to navigation) CMMURMVA V.M. ChoWes in sertm proteino in bronchogenic cancer. Terap.oth. 32 noall&77-W N 160. (MRA 34d) le Iz kafedry fakulltetBkoy torapii (say* - profe D.Do Tablokor) i kafedry bickh4mii (sav. - prof. L.Do Kuhevnft) Tm&ogo zedi. toinskogo imatituta. (BUDD PRMIIM) (NOCHIIL CUCIM) CHEBURANOVA, - CAND MED SO-l 9 "ELECTROPHORESIS OF -'BLOOD CAN Tom S K I LP~0TEI,NS .-- 4i~ SERUMJIN PRIMARY LUNG CEER," 19610 (NOVOSIBIRSK MED INST). (KL-DVo 11-619 230). -295- PAUTOV, A.V.; Y=V, P.Te.; CHBBURITSVO G.M. Regenerating silica gels for drying apparatus of turbocompressors vithout electric air heating, Prom.energ. 12 no.8:18 Ag 157. (MIRA 10:10) (Drying apparatus) CMkWtNMF-V.Q., elesarl fool for cleaning reinforcements from rust. Suggested by T.G.Chabursev. Rate.1 lsobr.predl.v strol. no.11:14-15 159. (HIM 13:3) (Reinforclos ban-XIsaning) CHEBURKIN, A.V. Use of preparations of the phenothiazine series in pediatric practice. Vop. okh. mt. i dot. 7 no.2:13-16 F 162. (,',rfu 15:3) 1. Iz detskogo otdeleniya goopitalya (glavnTf pediatT- kand. rmd.nawk G.N. Guzhiyenko). (MNOTHMINS) (FEDIATRIGS) CHEBURKM, A.V.; GROMOVA, R.V. Clinical anatomical parallels in neurotoxia in childrene Fediatriia 41 no.5:72-75 MY 162. (KIRA 15:5) 1, Iz kafedry detskikh bolezney (zav. - deystvitelInyy chlen MM SSSR prof. G.K. Speranskiy) TSentrallnogo instituta usover- sherwtvovaniya v3~aehey na bass Klinicheskoy detskoy bollnitsy Fo.9 (g~avz" vrach A.G. Kudrrwheva). (NMVCYUS SYSTM-DISEASES) (CHILDREW-DISMES) ACC NR- AP1002425 SOURCE CODE: AUTHOR: Rozanov, A. G.; CheburkiN N. N. ORG: none TITLE: Measurement of the electron concentration in a pulsed xenon discharge wit the aid of a gas laser SOURCE: Optika i spektroskopiya, v. 21,'no. 6, 1966, 761-762 Ta-DIC TAGS: laser application, gas las#r, gas discharge, xenon, discharge plasma, plasma densityheliumpeon.laser ABSTRACT: The authors constructed for the measurements the laser interferometer first proposed by H. Kogelnik and D. Ratel (Proc. IRE v. 50, 2365, 1962). The operation and theory of the interferometer are briefly reviewed. An He-Ne laser operating simul., taneously at 0.63 and 3.39 p was used in conjunction with an experimental plane flishi lamp filled wfth xenon at 40D mm Hg. 7M per udt energy in the lamo uTw go 'bules/CM3 and the tuerferoue= SenSUiVity Was 6.3 X 101" CM-3 per modulation peak. The results of meaGurement of the plasma density at different points of the discharge indicate that the discharge chan- nel is complete3,y filled. This was confirmed by direct photography of the discharge. The laser beam modulation of the plasma (number of modulation peaks) was constant from flash to flash. The time variation of the plasma density is similar to the variation of the dis,dune current. The maxi roumdensity, corresponding to maximum current, is 7 X. 1017 ce - The corresponding temperature at the maximum (calculated using the Saba formula) In 9500K,, and the degree of ionization is 5.4%. orig. art. 2/2 UDC: 53T.523/.52T ACC NR: APM2425 bas 3 flVnvs am 4 fcrua&ao SUB CODE; 20/ SIM DATZ: oksep65/ OTH RZF: 003/ ATD PRESS: 5113 MMURKIII, P.V. M.W-- Rare case of perforating wound of the thorax, Khirurgiia Supplement: 10-11 157, (KIRA 11:4) (CMT--VWM AND IWMIIS) z ZOINOVICHO D.P.; ZAYATSv Aele; JIUDNITSKATA, K,B,,t CHEBUKINA, L*Ke . Separation Of Cr3+ frcs iron by crystallization of ammonimi- chrme alvm., Zkure PrM, khis, 38 no*5:7?9-997 My 165. (KIRA 18:11) **A A f. A-L-IAA.-A-A-ALA a it Q t w 4 1. 1. AA MCC wtLis It I d I c fell, 00 so., 66 c 00. 1 alki 104441mirus.17,14! 70071. 1, 1 1 N't, piottin .11. ~,., Itmained The filukn Imth. 11- W41ftW AftCf CUU., CVU19. RbMt SnOtrin. WAS C-umniw, a'k-Rim amf thVittint, .~, ",tsti- 101kill 41"feally ti'miIIIII a nwhiv acad Got og~ kv so is t --9 s 4 "D- V- I t a ad o a a I w a a 2 It o d a a 4 9 n i a :do 0 0 1 0 00 00 0 0000060 0 0 a -00 see 00 C-"ErJORKWA) W_V, USSR/Biology Plant pathology Card 1/1 Pub. 22 - 40/47 Authors Ryzhkov, V. L.; Kabachnik, M. I., Hemb. Corresp. of Aced. of Sc. USSR; Thrasevich, L. M.; Medved', T. Ya.; Zeytlenok, N. A.; Harehenko, N. K.; Vagzhanova, V. A.; Ulanova., E. F.; and Cheburkina,, N. V. Title Biological activity of alpha-aminophosphinic acids Periodical : Dok. AN SSSR 98/5, 849-852, Oct 11, 1954 Abstract : The biological activity or alpha-aminophosphinic acids (toxic when in large concentrations), is discussed. The biological activity of these acids is beat expressed in the inhibition of virus multiplication in the mosaic disease of tobacco. The effect of these acids wA glycol on the titer of influenza virus in growing chicken enbryos Vag investi- gated and the results are described. Eleven references: 7-USSR; 2-USA; 1-French and 1-Ger-n (1930-1953). Tables. Institution : Acad. of Sc. USSR, Institute of Elementary-organic Compounds and the Academy of Medical Sciences USSR, The D. I. Ivanov Institute of Virus- ology Submitted : July 7. 1954 he D-upp on of plago a-fih-o-s- d VOLUY*AU, Te.N.; CHEBURKINA, N.V.; TOVARNITSKIY. V.I.; NIZOL'SKLYA. I.N. Isolation and chemical composition of symossn. Vap.med.khlu. 5 no.z:i4j-i48 *-Ap 151. (KIRA 12:5) lo Biochemical laboratory, 111.1.Ivanovoklym Institute of Virusology. Aeadesty of Medical Sciences of the U.S.S.R.e Moscow. (MAM. symossue Isolation 4! cheme (Run)) (POOMCCURIM, Sam) UGOLEVA, N.A.; BF-SKINA, S.R.; qHEBURKINA, N.V.; NOSACHEVA, A.D.; SLAVKO, T.D. Study of the infectivity of P14A isolated from tissue infected by Sendad virus. Vop. virus. 9 no.2-.184-188 Mr-Ap 164. (MIRA 17:12) 1. Institut virusologii imeni Ivanovskogo AMN SSSR, Moskva. CHEBURKINA NO.; ZAKSTELISKAYA, L.Ya.,- SLAVKO, T.D. Metabolism of nucleic acids In developing ohick embryon infected vith influenza viruses. Vop. virus. 9 no.6t670-674 N-D 164, (miRA iB:n) 1. Institut virusologii imeni D.I.Ivanovskogo AMN SSSR, Moskva* CHEBURKINk, YE. M. *Complex Utilization of the Electric Motor In Agriculture.* Thesis for degree of Cand Technical Sci. Sub 27 Jun 50, Moscow Inst for the Mechanization and Electrification of Agriculture imeni V. M. Molotov Summary 71, 4 Sep 52, Dissertatim fty Moscow in 1950. From Vecherniava Moakm, is c 1950. fVj , CHEBURKINA, Yoo, knndidRt toldinichask1kh nauk, "'~- 'A ~ us Ce rtric ;~~vlng of food grinders and cutters for livestock fnrms. Much.grudy VDW 2t:70-85 156. (KLRA 10:1) I (Electric driving) (Food grinders) CRIBURKIIU, Ye. M. Loose housing of cattle in Sweden. Sbor. nauch.-takh. inform. po elek. selikhoze no*7:58-61 159* (HIM 13:9) (Sweden-Wz7 barns) ' -to 0 1 1 14 It 11 to It A I ), 1) 11 A is A17 11 w It u it u o 4 1! P. A 1. it 1_1 1. v V I AA a Et W tt CHEOORKOV) A- K. zoo _-0o =00 go zoo Of go Z0.0 00 loo 0 01 -00 '00 40 00 L L GO I*L%VPUK&L LIVIN G Ickawspocallob woo .1,431 C.. it, too U_ ' , a *001 oo";t *Tz : 401*0000 IAI $IlIwo -1 00:~10*4000000*000* 04; 0 0 0 0 0 0 of 0 0 0 o 00060000 00,000000000000000 04 RUSTER, Semen loopolldovich; GARASHCEMED, Aleksandr Petrovich; -nHUUR=T-A-&K.-. Inzh.. reteenzent; GLIKIN, N.M., Inzh., red.; SMSHURINA, Te.A.. red.lxdatellatva; BLIZIND, V.D., tekhn.red. [Squipment. automatization and sechanization In plants for heat treatment of aetals] Oboradovanie, avtomatizatalla I sekhanizataiia v tormicheakikh teekhakh. Izd.2-oo, perer.1 dop. Moskva. Goo. nauchno-tekhn.isd-va mashinostrott.lit-ry, 1957. 391 P. (MIRA 11:1) (Metala-Heat treatuent) 137-58-4-7606 Translation from: Referativnyy zhurnal, Metallurgiya, 1958, Nr 4, p 177 (USSR) AUTHOR: Cheburkov, A. K. . - TITLE: Heat Treatment (Termicheskaya obrabotka) PERIODICAL: MashinostroiteV, 1957, Nr 8, pp 18-22 ABSTRACT: Experiences in the development of procedures used in the heat- treating shops of GPZ Nr I are described. Pusher furnaces re- placed shaft furnaces for the annealing of forgings. This made it possible to free more than half the total floor space, the anneal- ing cycle was reduced from 48 to 18 hours, the consumption of electric power per ton of forgings was reduced by 15 percent, and th61 quality of the heat treatment of the forgings was improved. Special dies were used to harden large bearing races. To avoid spontaneous increase in race size after the final finishing opera- tion (a ball race may "grow" 104.15 microns per 100 mm diameter over a 6-month period) induced by gradual transformation of un- stable retained austenite to martensite, two methods of stabilizing the dimensions are employed: the cold- temperature working meth- od and the heat method (used for wheels the RC of which may be Card 1/2 60 or less). All ShKhl5 races are washed with cold water before 137-58-4-7606 Heat Treatment tempering. Another method of stabilization is based on the decomposition of the retained austenite when tempered for 3 hours at 2250C. However, this meth- od is accompanied by a reduction in hardness. The following pretreatment to increase the stability of the martensite is performed in order to maintain RC at 60: forgings heated to 900-9300 are cooled in a stream of air until they dirk- en, and are then annealed at 8000 (2 hours) to produce a structure consisting of fine grained and punctuate pearlite. 1. K. 1. Heat treatment--Equipment 2. Furnaces--Applications 3. Ball bearings --Heat treatment 4. Metals--Heat treatment Card 2/2 SO'%~/l 37--59-2-4370 Translation from: Referativnyy zhurnal. Metallurgiya, 1959, Nr ?, p 291 (USSR) AUTHOR: Cbcburko-,z, A. K. TITLE: Heat Treatment of Bearing Rings (Termicheskaya obrabotka kolets podshipnika) PERIODICAL: V sb.: Materialy Soveshchaniya glavn. metallurgov z-dov i in-tov avtomob. prom-sti, Nr 3. Moscow, 1958, pp 22-25 ABSTRACT: To ensure the fulfilling of the plan, shaft and box furnaces are introduced at the First Bearing plant for thefollowing heall treatment of large bearings-, hardening, carburization, and tempering. The hardening of rings in the "press machine" ensures dimensional sta- bility and, therefore, affords a decrease in the depth of the carbu- rized layer and a sharp increase in the output of the carburization furnaces. The e'quipment of the heat-treatment shop is being modern- ized and work is being completed for putting into action new instal- lations for heating with HF current for quench-hardening of self- aligning bearings. The author notes a number of measures being carried out at the plant to increase the efficiency of the heat-treatment Card 1/1 equipment. A. B. RUSM, semen Leopolldovich, kand.takhn.nouk-.~'GARASH,CEUINKO, Alek- sandr Petrovich. [Urn shchanko, 0 P. 1, lmand.tekhn.nauk;-CHISUR- KOT,A.I. insh. retsensent; GLIKICNALMikin. N.M.]. ra;7.- l2quipment, automtIon. and machanistion in heat-treating departmontal Obladnamda. avtoawtyzataiis I makhanl2stalis v tormlcbnykh teekhakh. Moskva, Darzh.naukovo-tekhn. vyd vo gas ynobudIvaol Ilt-ry, 1939. 371 p. (MMA .14:5) (Autoitation) Obtals-Reat trestmut) G'.hfiriges In tho f' C.- c .'079 N-Yo, klmdet4khnoaamt; IGRATIMMA. 16P.. Insh. Bulldlog apffus mdo of wast4a obtalued In produclug bWdrofluoric acid. Strol. sate 6 noslo#36 0 060o (MM 23:10) (Gyp=) CEMKOV, M.F ; YEGOROVAR A,M. Sow properties of agleperite foam fly ash concretes. Trudy Ural* politekh. inst. no.ns:52-59 162. (MIRA 16:6) (Lightweight concrete-Testing) CHimKOVI N.F.; KAIMMI M.N.; FIYACHEVA, O.Ye. "ftftftm=mmWWW--~ use or light ashes from electric power plants to replace c14" r cemeba In factory production of concrete and roln- forced concrete products. Trudy Ural. politokh. inst. no.118:70-ft 162. (MM 16W (Asb(Toobnoleff)) (Pkvcaot concrete) CHEMKOV. M.F.; KASHIMKIY,, Yu.A.; TUNGUSKOV, A.S.[doceased] fflm~ Studios of emeretes and reinforced concrete elements made with portland cement vith an additive of pulverized ash, Tnidy Ural. politelch. inst. nooll8885-95 062, (MMA 16:6) (Concrete-Testing) Ash(Tecbnology)) trtland cownt) PIYACHFVq V.A.; CbTBUKOV..-,-.M.F. Dic-liromate sludge as a raw material. for the production of cements. lzv. vys. ucheb. zav.; khIm. -11 khIm. takh. 8 no,lgll8-123 165. (MIRA 18g6) 1. Ural'skly politeklinicheskly institut Imeni Kirova, kafedra tek'anologii 111sementao 6/844/62/OUO/000/025/129 D244 D307 AUTHORS: Cheburkov U F Nalakhov, K. V, Gramolin, V. A. and TITLE: Influence of the variation of the quantity dE on the dx yield of nitrate ion on aqueous nitrate solutions SOURCE: Trudy 11 Vsesoyuznogo soveshchaniya po radiatsionnoy khi-, mii. Ed. by u. S. Polak. Moscow, Izd-vo ?1N 6-0-SR, 1962, 159-161 dB TEXT: The authors investigated the effect of decreasing - U-x Of the applied radiation on the yield ofnitrite in nitrate solutions. 6olutlowj containing 0.01 - 6.0 g - ets/1 NaNO 3 and Griss reagent were irradiated by A- rayu from a Co 60 s'ource, 14.1 Nev neutrons and ~A-particles from Pu239. It was established that in dilute solutions of NaNO3 (0.01 M) the yield of N02- depends strongly on quantity dE .- . In 0.1 and 1.0 1-1 solutions the yields for the various methods 6/844/62/000/000/040/129 D214/D307 AUTHOR6: Malakhov, K. V., Cheburkov, 0. F. and Kabakchi, A. M. d- dyes SOURCE: Trudy 11 Vsesoyuzziogo.sovelshchanlya po radiatsionnoy khi- mii. Ed. L. J. Polak. Hoocow, Izd-vo AN 666R, 1962, 243-246 TEXT: The uction of 4' rays (Co 60 source) on aqueous solutions of methyl orange and phenyl red was -studied..This radiation caused an irreversible decolorization of these solutions. The color, before or after the irradiation, was stable tD daylight and to air. Ojjtical~" density of tl-ie dye solutions was proportional to the absorbed *energy" and all results were obtained. by measuring the former. A 5 x 10- 6 111 6olution of methyl orange, at p1l 2, gave a constant decolorization yield in dose range 10 - 1.5 x 103 rad; a 5 X' 10-5 1-1 solution, under the same conditions, gave constant yields in the dose range of 8 x Card 1/2 TITLE: The action of radia!"Jon on dilute aqueous solution s o.f S/137/61/000/005/056/060 1, t L) A0061AI06 AUTHORS-. Bychkov, Yu. F.; Rozanov, A. N.; Skorov, D. M., and Cheburkov, V.I. TITLE: Corrosion resistanoe of 11-T (Yal-11) steel in lithium with oxygen and nitrogen admixture PERIODICAL- Referativnyy zhurnal. Metallurglya, no. 5, 1961, 60, abstract 51453 (V ab.: "Metallurgiya i metallovedenlye chistykh metallov", no. 2, Moscow, Atomizdat, 1960, 78-92) TS'v1 The dut-hors studied changes In the microstructure and mechanical properties of Fe, N1, and Cr-Ni- steel grade '~Y&I-V' as a result of the effect of distilled Ll and 111 const-aird-ng 1-2 weight % 0 or N. They investigated also changes in the chemical composition of Li due to the corrosion of the enumerated substanaes contained in it. Ye. L. [Abstracter's note: Complete t.--anslation] Card I/I BYGHKOV, Yu.F.; ROZANOV, A.K.; GROMOV, B.I.; CHUMOV, -Y.I. Laboratory equipment for the vacuum distillation of lithium with a complete filling of the crucibles. Met. I metalloved. chist. not. no. 2:171-177 160. (MIRA 13:12) (Litbiw*-Motallurgy) (Metallurgical laboratories-knipment and supplies) .CHEBURROV, Yu*Ao; BMAMOVA, M.D.; KNUNYANTS., I.L. dt-Hydrohexafluoroisebutyric acid fluoride as a now system with a mobile hydrogen atom. Izv.AN SSSR.Ser.khim. no*2.4367-368I F i64:; (MIR& 17:3) 1. Institut elemsixteorganichaskikh seyedineniy 0 SSM t./pleparau-m- of al"~':d of th~~ furan1dine "Tim Yu. A. C It churkov-,,dr --T -70 0 Gua, 2 lactt- lykne, 1-5g. 30, and'.4 -xingsh, w Irg Ion WIM) If--S, -Tashing with NkC-O~ and H,O,, 7450 '2,2,5,5 1 *,41 d.,, 00~~ b~manei mi. 21,1-151; imvtr~ in. 1281). D?.H In 5 till, r -55VO -, r 100-P. 1 (115 g') and 16.0 g. dioxane-Bri shaken in the 66ld .1 lim pvc ?Jttr washing, 9470 4~-brorso deriv., nj?1.5250, d1a 1.2030. Re. -g. fluxing 10 g. I Uith a Re% in 11N), ml. dioxane and 5 tnI " 11.0 (the initial tnixing bcir_.- made dropwise) 12,hrs, gave nrzova! of Se. distr of dioxanc and extn with McO bt. -167-70'. in. 69m-70%:rcd; 'kept in -T-T,O it 0owly Otis HO and formscolarlesicry-tals; wbich tun loss of HIO on hmting- diciri~- M. IS2.5-31. Refluxing,80 g. b)-(l- ljydrox)~""Clopmty , N -1)-icit Acne, IM g, 11%0, and 33 g.-VgSO, MCI vd civer O.G tir.) 15 brs-ga,~c nitu extn. %vith M-0 69% 4 111,5 12 nV 1AKH5. d ni. 'M . IT Ivith JIM in the -pr~~enct of: N1111TI, A- abDre' pvc. 4,3% zylid- . t4 %7'1111 S-Oz ill dioxatle 12 Tits.-gave b:1 7133-4W. m, 37% md; form color- M T '4-DIkotonts of L. -It h e sy-j th e 5i5 0i / 7, Z- j z % j YI V- culos Of b1sply"Wo type I' "u JAN LFIIIY,, M., IN -63Q2kqu cl. C-4~ 49, 31976.-Heating 0.0 g. 2,2,5.E-bisprntamctliylmeftimnidinL,3,4-(Iione (1) and 0.27 g. o-C&H4NIH02 15 rnin. gave 90% 2,1,4.4-1~--.'s- 117.2- 17.5'.. 5-nilnrly. was prepd. 907o 2,2,4,4-b~s.Ic1rGmt1hYIrnc- -105.5-6.0'. from I and (C11- , NH-)01:0 b6ated briefly, taken up in EtOll, and tTeated 1,2.4,4-;bispertatrelh3~ieneftira io- with :H~O gavel 92% Hid r -6 7-d-'Y,?roP I~rcj In. 64'.1 . Similarly 11 gave 79% ) = N147-8',n'D'LW953"d=I.09W. I(lI.8g.)rduxed2hrs. in 100 ml. AcOffvnth.1.4 Z. urotropine and 25 g. AcONH4 gave,after quenching in ice, filtration j and satn. with,M]'j. Ohykn, urar 81% 4, t 6,6-bispentan, -ef idiw43,4)imidaE4e, M. ' in. 244,5-5,5* [from (cl-12CIA.r ' i (2-S LOG- v, 1341, and 10 g. AcONH4 treatc~lasabove gave. 'imidazole, in. 230w-M.Sc (from C,H,). simil !y gave 951" ar '0 air,) I,N e" ' ' 41 - 4. .1. C, 1~ 204.64.5'! (from dit.'MOII). . 18 g, semi- (1 _J 10inl-AcOlliefluxed'I hr. and qv i ci cbe -gave'w%-Lmonosemicarbazone, rn. 18-2.5-3.5', (0.5 g~) telitia d n 4 % 0 3 hrs. ubitti 0 Ma ac idificiitlc~i AcOH 76% (Ila, R - 011), ni. 214* (from ~ctr. Oher). 11 as -above gave 65% 3~hydraxy- -I1CV and OM g. thiosemi=baxide ill 6 tal, -e 85% 11 tno o1hio- 6tidlic and 1 int. H%0 rm zand,10 W. AcOli I Imi Mlowed by 90 xuL 406,',0 NaOll and 'x his rentaing Z j. gave 76%, m 104-6', St"Milarly I gave on fopuxing with W and AcOH a low yield of Ila (R -SH) (IV), in. and a more sot. I -nonoth-'03MI.- A bove cqr~a;xje, the latter refluxed 2 hrs. with 4~~" NlaoH gave g% good yield of IV. -G ~~ 6 oo 5.3 77292 SOV/63-4-6-26/37 AUTHORSt Knunyants, 1. L., Rokhlln, Z. M., partbax-tan, N. P., Chaburkov, Yu. A., MIA ch'IngyWr--- I Brier. Communications. Pluorinated Ketones. Bin- (trifluoromethyl) -glycolic Acid tZRIODICALs KhImIcheaksym naukA I romyshlenno3t-, 1959, Vol 4, Mr 6. pp 802-804 (USSR 3 ABVMACTj Nltrile of b1 s-(t rifluorome thyl) -glycolic acid (:r) t was syn healred by the reaction or hoxachicroacetom, with HCH In the presence of a catalytic amount of i ldI ne. per p piparldin (Cp ) C~O CO + HCN H (CV ) T) - 2 3 2 CM 3 M can be distilled at atmospheric pressure without d 0 :comp sition but, In the presence or piperldine, (1) decomposed to HCN and haze ri uo rose atone. (1) Is partially hydrolyzed In the presence or water at rocn. Card 1/4 ta"raturt, forming hezarluoracetone hydrate and lic"I. A330CLATION: Xn3tLtute or Element-Organic Copound3, Academy or/scien" 0, USSR (Institut elementoorganicheskikh doyedi-nenty Akademil nauk S=R) SUBMITTEDt July 18, lq~q Card 4/4 AV S/062/..60/000/008/031/033/xx B013/BO55 AUTHORS: Knunyants, I. L. and TITLE: Some a-Amino Acids Containing Trifluomethylene Groups PERIODICAL: Izvestiya Akademii nauk SSSR. Otdeleniye khimicheskikh nauk, 1960, No. 8, pp. 1516-1518 TEXT: This brief communication treats the add'ition of ethanol amine and diethanol amine to the ethyl ester of Ptp-ditrifluomethyl acrylic acid. Under mild conditions, the reaction with ethanol amine gives N-(P-hydroxy- ethyl) hexafluo valine ethyl ester. Only the amino- and not the OH group enters into reaction, though alcohols react equally readily with fluo olefins, specially in alkaline medium, The structure of the product was confirmed by synthesizing it from the hexafluo valine ester and ethylene oxide. The reaction can be carried out at room temperature in 50% acetic acid. With thionyl chloride, the N-(P-hydroxyethyl) hexafluo valine ester is readily converted to the N-(P-chloroethyl) hexafluo valine ester (II). The latter is transformed to the water-soluble N-(P-chloroethyl) hexa- fluo valine (III) by hydrolysis with hydrochloric acid. Diethanol amine Card 1/2 Some a-Amino Acids Containing Trifluomethylene S106216010001008103110331XX Groups B013/BO55 did not react in the corresponding manner, even on heating to 1500C. The authors assume that the cause for the absence of an addition reaction between diethanol amine and Plp-ditrifluomethyl methacrylate is to be sought in the steric hindrance due to the carbalkoxy groups, which prevent the di-(P-hydroxyethyl)-amino group from entering the a-position. At present, the biological activity of hexafluo valine and its hydroxy- ethyl- and chloroethyl derivatives is being tested. There are 2 references: 1 Soviet and I US. ASSOCIATION: Institut elementoorganicheakikh soyedineniy Akademii nauk 33SR (Institute of Elemental Organic Compounds of the Academy of Sciences USSR) SUBMITTED: January 22, 1960 Card 2/2 S10621601o0c; -'0 12/039'/020 B013/~055 AUTHORS: Knunyants, I. L. and_Phebukgy.Xu. A. TITLE: Unsaturated Acids Containing Trifluoromethyl Groups. II. Free-.radical Addition of Hydro.aen Bromide to O,O-Di(tri- fluoromethyl)Acrylic Acid PERIO`1IC1%L: Izveatiya Akademii nauk SSSR. Otdeleniye khimicheskikh nauk, 1960, No.12, pp. 216a-2172 TEXT: The free-radical addition of hydrogen bromide to P,P-di(trifluoro- methyl)acrylic acid was realized in the present work- Dry hydrogen bromide adds to P,P-di(trifluoromethyl)acrvlic acid (I) both under the conditions of a:f~ee-radical reaction and without addition of an Initiator (in presence of an inhibitor), forming P,P-di(trifluoromet,llyl)a-,orobi,omo propionic acid (II) in high yield. In order to establi3h the structure of (!I), the authors tried to substitute the hydroxyl group in the previously pre-oared (Ref.-3) ethyl ester of a,a-dihydroperfluaro-P-hydroxy isovaleric acid (III) by bromine. (III) reacted with phosphorus tribromide onl,,, under extreme conditiDns, forming (II) but also P,P-di(trifluoromethyl)acr-.-lic acid and ite esters (IV) Card 1/3 Unsaturated Acids Containing Trifluoromethyl P62/60/000/012/009/020 Groups. II. Free-radical Addition of B013/BO55 Hydrogen Bromide to P,P-Di(trifluoromethyl) Acrylic Acid owing to the occurrence of dehydration under these reaction conditions. (III) reacts with thionyl chloride in presence of pyridine in a similar manner, a,a-dibydroperfluoro-p-hydroxy isovaleric acid reacts with an equimolar amount of thionyl chloride under dehydration, forming P,P-di(trifluoro-- methyl)acrylic acid, whereas with 2 mole thionyl chloride or phosphorus pentac~loride it forms the acid chloride of P,P-di(trifluoromethyl)acrylic acid (V) which isidentical with the product obtained by treatment of W with thionyl chloride. The splitting off of water from the hydroxy-acid eater (III) under the action of thionyl chloride, which takes place under comparatively mild conditions is a somewhat unusual reaction, since the dehydration of compounds of the type R R --C-CH -R; F 1 '2 OH is known as difficult, Introduction of halogen into the P-position (re- lative to the carboxyl) of P,P-di(trifluoro)p-,proDiolactoiae by means of phosphorus pentacbloride also gave P,P-ditrifluoromethyl acrylic acid Card 2,13 Unsaturated Acids Containing Trifluorometbyl S//062/60/000/012/009/020 Groups. II. Free-radical Addition of BO13/BO55, Hydro gen Bromide to P,P-Di(trifluoromethy Acrylic Acid chloride. The structure of (II) was confirmed by hydrolytically splitting of the halogen at 135 0C with water, whereby P,P-di(trifluoromethyl)-a-hydro- xy propionic acid (VI) was obtained. The latter resembled the acid obtained in Ref. 1. The addition of hydrogen bromide to 0,0-di(trifluoromethyl) - acrylic acid proceeds by a radical mechanism. The reaction is catalyzed by peroxide and ultraviolet irradiation and inhibited by hydroquinone. Of the two possible intermediate radicals A and B formed during the attack on the double bond by the bromine radical, the free radical A is the more stable. This is in agreement with the data indicating that fluorinated tertiary radicals are more stable than secondary and tertiary radicals (Refs. 8, 9). There are 9 references: 3 Soviet, 4 US, and 2 British. ASSOCIATION: Institut elementoorganicheskikh soyedineniy Akademii nauk SSSR (Institute of E-lementa'-organic Compounds of the Academy of Sciences USSR) SUBMITTED: July 2, 1959 Card 3/3 KNUNXANTS, I,L.;_CH~~RKOV, U.A. __I_ t orine-conta4n' 4-lactomm. Mport No.2: 4-triflummtby.1- -mtbyl-Aproplol:actonso Isv*AN SSSR.Otd.khla,nauk no-5:808- A sio )w 961, (KIRIL 1425) I& lmtltut el~ntoorganlchesklM soyedineidy AN SSSR. (Vydracrylic &aid) m I KMNrANTSj I.L.; CHEBURKOV, N.A. Morine-couuin~x~iacto~l 2actows. Revitt 110.3: Reactiom of opeoft fowmwmbored- ring of /1-trifluoreamthyl-tt-nothyl-,4-propiolactone. Isv*AN SSSR.Otdokhin.nauk no~5:8n-W my 161. (KMA 34:5) le Izwtitut alowntoorgwdchoskikh soyedluenly AN SSE. (Bydracry3-tc acid) KNUNYANTS, I-L-;_PHEBURKOV. Ya-A- Unsaturated acids containing trifluoramethyl groups. Report 3: Polikrization of the doable bond in /I -trifluoromethylerotonic acid. ImAN&SMAWAhimonauk Ao.6slO57-1062 J9 161e (MA 14:6) 1. Institut elementoorganichookikh soyedineniy AN 3 M (Grotonic acid) MFMMUM a I.L. I; CHEBURKDV, TuA.; MAKAROV, Yu.To Mwrnl decomposition of alcoholates of tertiary alcohols containing trifluorawthyl groups. Izvo AN SSSR. Otd.khis. nauk no.8:3.471-3475 Ag 161o (KM 34:8) 1. Institut elowntoorgonicheskikh sayedinfmiy AN SSSR. (Alcohols) (klc&olatea) KNUNYANTS, I.L.,,'akademik; CHEBURKOV, Yu,A, Mudfestation of pseudobalogen properties by a trifluoreomtbyl group, bound to a carbon atom. Dokl-AN SSSR 1,37 no-5.-IM-1124 Ap 161, (Trifluorometbyl group) (IMA 14:4) .%A.L; BARGAMOVAv M.D. KNUNYANTSv I.L.; CHEBURLOVa.Yu . onethacrylic acid. Report No.111 Perfluorodewthylketene and perfluor Hexafluaroisobutyric acid halides from fluorinated ethers. Izv.AN SSSR.Ser.khim. no.8tl389-1393 Ag 163. (MIRA 16:9) 1. Institut elementoorganicheskikh soyedineniy AN SSSR. (Fluorine organic compounds) (Ketone) (Isobutyric anhydride) KNUNYANTS, I.L.; CHEBURKOV, Yu.A.#- BARGANOVA, M.D. Perfluorodimthylketene and perfluorowthacrylic acid. Report No.2: Comparison of ok -hydrohexafluoroisobutyric acid halides in the reaction with triethylamine. Izv.PN SSSR.Ser.khim. no.8:1393-1397 Ag 163. (MM 16:9) 1. Institut elewntoorganichaskikh soyedinaniy AN SSSR. (Ketene) (Fluorine organic compounds) (Isobutyric anhydride) (Triethylamine) CHEBURKOV$ YUiAj; MYSOV,, YeJ.; KNUNYANTS, I.L. Perfluorodimethylketene and perfluoromethacrylic acid. Report No.3: Comparison of haloan)Wdrides ofac, -halobexafluoroisobutyric acids in the reaction with zinc. Izv. AN SSSR. Ser.khim. no.9:1570-1572 S, 163. (KUU 16.- 9) 1. Institut elementoorganicheskikh soyedinertiy AN SSSR. (Ketene) (Propionic Mid) (Zinc) ACCESSION NR:.AP4ol9ol6 S/0062/64/000/002/0367/0369 AUTHORS: Cheburkov, Yu. A,.; Bargamova, M. D.; Knunyants, I* L. TITLE: Fluoroanhydride of eL-hydrohexafluoroisobutyric acid - a new system with'mobile hydrogen atom SOURCE: AN SSSR. Izv. Seriya khimicheskaya, no., 2, 1964v 367-369 TOPIC TAGS: hydrohexafluoroisobutyric acid, hexafluoro pivalic acid, bromohexafluoro isobutyric acid, mobile hydrogen atom, fluoroanhyd- ridel structural formula ABSTRACT: This is acontinuation of an earlier work by the authors (I~v. AN SSSR, Ser.. khim..1963, 1393) in which they described the remarkable properties of the above product. The purpose of the preaent article is'to chose between two structural alternatives for it, namely: %*CjH6 ACCESSION NR: AP4019016 'After a discussion supported by reactive evidence, the authors expressed preference for -the second alternative formula, although they admit the possibility of existence of structure I. Spectro- scopic investigation was inconclusive. During the course of thii investigation, the following products were prepared; and fluoroan- hydride of hexafludropivalic acid, ethyl ester-of their ch4racter- istics described: -.Pt -bromohexafluoroisobutyric acid.. Orig. art. has; 6 Zformulas. ASSOCIATION: Institut elementoorpnicheakikh so edineniy, AN SSSR (Institute of Elementoorganic Compounds AN SSNT 19ju163 DATE ACQ: 27Mar64 ENCL: 00 SUB CME: imm i HR RE? SOV: 003 OTHER:-000 M? L- 169 RPL Oi-Vhe-4 5_2_45 OrWroVERWA-FRAW _S/(W2/6h/00q/0D6A526/JL520 M P5OD28-14 ul- ambAgeng ~,No pq Chebiwkov AUTHOR 1 6 nts, hexa uorac TITLE: Pinfloon rom ,t~ovji 1.964t 1526-1528 -j" SOURM AN WSR. 12vestiyP. Seriya khimicheakpYal no. 8p TOPIC TAGS: acetone, organic phdsphorus compol~nd, fluopinnted or&;-nic compour A tract.- Th6.teaction~of.bexafluoratetone with tri thylphosphite was inve.. t4gated. and. dodecaf iuoropinacol~jwae` synthe.aimed. Hexafluoracetone reacts vigorously% with triethylphosphLiento form:the 2:11 adduct, which is a saturam cyclic.phoephorane._ The strong eNectron-acceptor action of trifluormethyl- groups so weakens the basic'propertiea of fluorated pinacol that it does hot articipate in thepinbcol regrouping, P even upon prolonged boiling in 100% sulturic acid. Cycl ic, phosphora.ne waa' obtained by asding 32 grams of per-.,.,.- 'fluoracetone.to 16.8 grams..of triethy~phosphate* The product was 41.4 gratm 0 oint (0.5 am), freezing at -9 -~-80; oJoliquid with a -61-62, boilin& p nD 1.3555. Phosphorane is~a coloil ss--liquid, Lneoluble in water, soluble e -acetonej ether, and benzene. It' does not decolor Rft~% in alcohol,, Card-1/2 -N_ ROKHLIN, Ye.M.; ZEYFMAN, Yu.V.;,GHEBURKOV, Yu.A.; GAMMARYAN, N.P.; KNUMANTS, I.L., akademii ', - Reaction , h9x&flUoroaCGtOne 't,h triethyl phosphite. D&1. AN SSSR 151 no.6:1356-1358 AP 165. (MTRA 18'.5) 1. Institut el-ementoorganicheskilib soyedineniy AN SSSR. t-22 9 (I~guRk 2.800) CHEBURKOV, Y A.; MUKHAMhDALIYEV, N.; KNUNYANTS I.L. t Reaction of hexafluorolsobutyryl fluoride with acid chlorides. Izv. AN SSSR. Ser. khim. no.8t1476-1478 165. (mm 18:9) 1. Institut elementoorganicheskikh soyedineniy AN SSSR, CHEBURKOV, Yu.A.; MUKHAMADALIM, N.; ARONOV, Yu.Ye.; KNUNYANTS, I.L. Reaction of perfluorodimethylketene with dimethy1formamide. Izv. AN SSSR. Ser. khim. no.8tl478-1480 065. (MIRA 18:9) 1. Institut elementoorganicheskikh soyedineniy AN SSSR. _p 7,.j,A. , FXTIYAN-IS, Ltl,~ 141DRAAMAPP-LATENT;. H~,- ~gfq~4.ql y No.6c Rex-:vhiz'-.n ulth tives of ultrous avid, Im, ~k SOSSR. S-.r,, kh.ff . nw.lh1982-lqR7 165" OCRA 3601) 1. Twtitut AN SSSP~ KNUNYANTS, I.L.p akademik; KOCHARYAN, S.T.; CHF-,Bn?,'01,', Yu.A.,- BARGAMOVA, M.D.; RUMIN, Ye.M. Reversibel dehydrofluorination of 2-monohydroperfluoroisobutane and e-hydrohexafluoroisobutyric acid esters. Dokl. AN SSSR 165 no,4:827-830 D 165, (MIRA 1802) 1. Institut elementoorganicheskikh soyedineniy AN SSSR. L 17611-66 EWT(m)/EWP(j) WW/JWM4 ACC ITR: AP6002099 SOURCXCODH: UR/0062/65/000/011/1982/1987~ AUMORS i Mhkb~mWdal&evo N,.; Cheburkov, Yu, A.41 I, L. Institute for Heter io,Compounds, Academy of Soiences,SSSR (Inatitut elementoorganicheskikh soyedineniy "mii nikilk SSSR) ~TITLE: Perfluorodime o cation 6. Interaction with nitrous acid tene :d6rivatives :SOTIRCE.- AN SISSR. Izvestiya. Seriya khimicheskaya, no-11, 1965, 1982-1987 :TOPIC TAGS: -fluorideg.fluorinated hydrocarbon, fluorinated organic compound,, 41uorine~compound, organic nitrile compound, chemical "action !ABSTRACT: Me properties of the fluoroanhydride and ethyl ester of Ok-nitrosohexa-" :fluoro'butyric acid were studie&to extend the work of the authors (Dokl. AN SSSR ;165,1 (1966)). The latter compounds were.obtained by reacting perfluorodimetbyl- .ketene with nitrosyl.fluoride and othylnitride.1 In additiont.the reaction of perfluorodimethylketene with sod-1121n nitrite and' nitrogen, trioxide I yielding an oxime of hexafluoroacetonep was also stadiedo A reaction mechanism for each of the reactions is proposed, and the yield and melting point of each product are recorded# Card 1/2 1 iv Wt j Aaa- rk. AC~ NR% Soul~ffrl -CO~E-I-UR/0062/6 000 0 104,91037 L, BARGAMOVA, M. D., Institute of Hetero ~JG JL ASA Iormnic '.Compounds, By n? F--:Lences USSR (InStitut elemantoorganicheskikh i -j1Sd,y-ed1wniy AN SSM) "Aiiion of T#ethy3Ajpjne on HexafluoroisobutyUl Fluoride" livestlya Akadem Sauk SSSR,, Seriya Khimicheskayn, 10 6, i966,~~ W 110 -1057, 'Abstract: Dimer~zfttion ~r hexafiuoroisobutyry~ fluoride under the action of trieth:~Iamine'vaa demonstrated. The molecular complex$f hexafluoroisobutyryl 'fluoride with triethylamine (1:1) is the triethy-la-M-o-nI salt of the enol form )of the fluq#~e ., and evidently undergoes a rearrangemenN the triethylammonium isilt ~.f the hypothetilcal unsaturated perfluoro-beta-methylaUyl alcohol. The 111lattei dimerize4 upon further heating, yielding a salt of a bis-perfluorocarbinol,' which loseq ".fluorqphosgene and is converted to a mixture of triethylamine 'fluoride aild the triethylammonium salt of p,--rfluoro-(4-methyl-1.3-pentacliene-4 ..Carbi~noi). The properties and reactivity of the dimer and a number of deriva- tives'of alpha, beta-unsaturated gamma-hydroperfluorinated acids obtained from 'it were iurestigated. Alkylation of hexafluoroisobutyryl fluoride by allyl ,bromide'and benZY1 chloride proceeds readily in the presence of triethylamine; alkylation do~qs_nqt.,pccur-vith methylene iodide, 1, 2-d,44odoethane, iodo- benzene. / Orig. -art W-h[un- -4- ttmrt 7LJM?' TOPIC TAGS: fl-qorinated organic mpound, triethylamine, lkylation SUB CODE; 0 DMM 02reb66 / ORIG REF. 008 OTH REF: 010 7 / SUM c0 ICNR:. AP7,00072:6, SOURCE CODE: UR/0062/66/000/006/10 438' MNUNYANTS I. _~.J,`CMMOV. YUL- A., BARGAMOVA M. D. ~WDIW, E. I., PiriROVSIC4." I 'Institute or iipteroorga-ni-a-U-ompounffi-3-, _Acad My of Sciences USSR ,,,"Perfluorociiinqthylketene Communication 7- Structure of the Dimer" 'Moscow, Izzvestiya Akademi~ Nauk SSSR, Seriya Khimicheskaya (news of the Acade~rror ;-of Sc~ences USAR, Coemical Series).j, 14o 6, 1966, PP 1031-1038 ,Abstiact: Perfluorodimethylketene, in contrast to other known ketenes, forms a also produced by i1near dimer iP4~r the actioii of triethylamine - The dimer ,tVo other methodp:-J) the reaction of an equimolar mi.xture of hexafluoroisobut.Y- i~l chloride and qtjiy1amine; 2) by the action of t~iethylamin2,jor cesium fluo- ,.riAe on perfluorome~hacrylyl fluoride. In the latter case thelreaction mixture ~wds treated ~itli apthanol, yielding the methanolysis product of the dimer and ,also the known *th, y1 ester of hexafluoroisobutyric acid and the methyl ester ~of alpha-trifluoromoqtbyl-betap beta-difluoro-beta-methoxypropionic acid. The structure-of tbp dimer of perfluorodimethylketene as the bis-fluoride of per .fluoro-(elpha, alphe~, g-ma-trivethylglutaconicYacid was confirmed by its re ,,:actions ~nd infrared spectrum. The reaction mechanism proposed for the dimeri zation included isomerizatiob of the ketene to the more stable perfluoromethacry-- .lyl fluoride- A pew reaction was discovered: linear'dinerization of AmAtional-de- ~7ivatives of per4upromethacrylic and dirluoromethylenemalonic acids.~Origa art -~as: 1 figure,-9 f6rimLw and 2 thblos. ffJPRS: 37.02ff -TAGS z --fluorinated _'orzanic comnound- isomorization ACC M AP7006077 SOURCE CODE: Ui~/66~~/ 606100~13N51i~61 AUTHOR: Cheburkov, Yu. A.; Mukhamadaliyev, N.; Mirzabekyants, N. S.; Knunyantsj I. L. ORG: Ins-Vit~ Veo -VeeM6~ganic Compounds, Academy of Sciences USSR (Institut elementoorganicheskikh soyedineniy AN SSSR) TITIS: Reactions of perfluorodimethylketene with alcoholsi, amines, and acids SOURCE:. AN SSSR. Izvestiya. Seriya khimicheskaya, no. 7, 1966, 1265-1267 TOPIC TAGS: fluorinated organic compound, amine, alcohol, glycerin ABSTRACT: The reactions of perflourod:bnotliylketene with alcohols, aminose and acids were studied. These reactions are copmon both to perfluorodi- metaiylketene and to nonfluorinated ketenes and lead to the production of various derivatives of hexafluoroisobutyric acid* The reaction with alcohols yielded esters. In the case of glycerin, at room temperature ketene alkylated only tuo hydro.V Groups, either vicinal or terminal. .Gopipleto acylation was achieved only by heating the glycerin i4ith excess perfluorodimethylIcetene in a scaled tulbee The reactions of ketone with .amm.nia and amines yielded amides of hexafluorolsobutyric acid. In these ,reactions an excess of amines mustbQ avoided to prevent mineralization of the fluorine atom by splitting off-hydrogen fluoride. Perfluorodimethylketne reacted readilywiih hydrogen chloride or bromide and with organic acids, yielding acid halides, anhydrides, and mixed anhydrides. The structures of the the new compounds were confir=d by infrared and nuclear magnetic resonance spectra. Orig. art. has: 4 formulas and 1 table. [JPRS: 38,9671 SUB CODE: 07. SUBM DATE: 14Dec65 / 'CRIG REF: 009 Card 1/1 UDC., 542-91 + 547.233 + 547.26 + 541-452 +_546o1 ACC NR-t-AP7000727. 0062 66/000/006/1038/1047 SOURCS CODS i U11/0062 My6w M-%-z SJ:o L-0 CH MOW& A! A. AHONNB Yu. Ye., Institute of Hetero- orranic Go= unies USSR (InstAtut elemontoorganicheekM ipyodinoni.y AN =i) "'Reaction of Chlorides of Carboxylic Acidalwith DLmthjy1forv=dde" Moscow, Izvesti a Aka4pmii Hauk SSSHp Seriya Khimicheskaya., No 6, 1966, y Pp 1038-1047 Abstract: A nev trend of the reaction of halideo of carboxylic acids with -dim.ethyl.-Cormandde, leading to aldehydes of these acids, was demonstratedo ,7Depending upon tltq structure of the acids, either transamidation or aldehyde formation occurs. In the reaction of acetyl, trifluoroacetyl, isdbutyryl, n- .-peifluorobutyryl, and benzoyl chlorides with dimethy1formamide, the dimethyla- r -'mides--of the*6orresponding acids vere formed. In the case of n r -chloridelltogethe'r with the basic product, the dit~ethylamide of pe orobutMl-t I -Mr-m-icacAd was formed. -Xu the case of hexafluoroisobutyryl chloride, the re- ,action with dim6thy1formamide-liberated C02 and produced an unstable crystaMne .Substance, w1lich readily hydrolyzed to hexafluoroisobutymldehyde. Derivatives of hexafluoroisobiAtyryl chloride-and trichloroacetyl chloride reacted with dimOtby1fbrm=1de to form not only the aldehydes, but also the corresponding. .,ttiloroalkanes, and carbon monoxide,, decarbonylatign products of It-he original 7: -chlorides Trichlorowetyl. chloride reacted 6inultaneously according to the three schemes, rie'dina Ue dlwt~ylaxdde of trichlor%mmUo acid, chlorsl#-'aDd 1/2 UDC: 542~9~ + 2-951 5!L AFM -0717 reactiono of perf luor-opiva4l chl.oride and hexanuO-, --~ropiva'Xyl 621~ride qefe also studied. A general scheme.of the reaction of pkk1pri4s th d1wthy rmmLde vas propose&kt Origo arto hut' formi3m; and TOPIC -TAGSt: oarbwWU* add chloride, a1dehyde SUB COW 1 07 SM DATIC I 07D9o65 CRIG REFs 010 OTH REFs 010 2/2 ACC NR- Ap6035836 S01MCE CODE: UR/0413/66/000/020/0038/0038 INVENTOR:, Cheburlwv, Yu. A.; Mirzabelgaita,, N. S.; Knunyants', 1. L. ORG: none TITLE: Preparation of hexafluoroacetone oxime. Class 12, No. 18TO27 ~SOURCE: Izobreteniya, promyshlennyye obraztsy, tovarnyye znaki, no, 20, l1966, 38 TOPIC TAGS: hexafluoroacetone oxime, nitrosyl chloride, hexafluoroloo- butyric acid, i-ttAZI- *"/ f-W-~ -C;b j CIAJ~I&j ABSTRACT: To increase the yield and to simplify the technological process of the preparation of hexafluoro&cetone oxine vith the use of altrosyl chloride in pyridiue at lov tempera- tures, nitrosyl chloride is treated vLth boxafluarainobuty- ric acid, IPS) (VIA-50; CDE No. 141 SUB CODE: 07/ SUBM DATE: O5jul65 ,Card 1 A IA, Ye. Ye., Engr. Card. Tech. Sci. Distertation* "Not-onetallic lnc~usions in the Metal of a Welded Joint and YBthods -for Their DeterKpation." Central Sci Res Inst of Technology and Machine Building. - "TsNI17MASh." 21 Apr 47. SO: Vechernvaya Moskva, Apr, 1947 (Project #17836) Ila L a a 0 pia a I T W CA 0 c 9 v 6 a x 610 NO Lt?T~e g air ui~m P~s !T PTTT!, !I or cm &V a n 0 00 lob 04r ,valdiuvo UJAM AO) Wj%P a-111=19"111 MAI!) fee ,anpis,u atil III Jujifts j0 U01joultiuapp Joi p0 .1vaLu intall-V wo jo pui "iqujinji mulsing sq4 III PaJ40daA A1611OIA" IviatIs Q41 jo U0111%joiqP 3941 9160 ;0 P041&tu 9 AO XPMV 0 30 Blins" "-%I!) ' F Lqq-M 'd Wt6t &Unf '01 *A 'S Cu"Umm UV %=I" PIP" p PM MP " mw lop" apom 0-01~=n POW M4 lb "SpaquMmu 9 *0 r - 804. *0 *0 00 tingpdou dN* 91"13044 see 141(w) ON( any 111 7 00 " I -; a a 4 L; 61 01 a -zu!" a 4 1 T- .4 im, W My ChTnufu~OvA, YE. YE. PA 28/49T7 nan /djjjAj4VrY,' - BtUebn, DeteraInation of oct 48 Chemistry - Steels, Silicon Content of "Photi)6olor Imetric Method of Determining Silicon' In Iron Add Steel," To.-Te. Cheburkova, Con Scl Res Iast of Tech and Nwh.Constr, 3 pp OZavod lab- Vol 11vj No 10 Dlecasses subject method and. uses It to find silicon cohtent'In eight stools And two Irons. Results com- pare v1thIn *02% with grartmetric method. Method Is based on formatlo~ of.yellov heteropoly acid with m6lybdic acid, ?rhich forms molybdenum blue vhen oxidized by thin chloride. 28/49TT N CO skr Optanmw - FemOU0 Steel-Austanits %.gthod for Datez?dnIng -Nametallic Impuritles 7.SA.Avptanlte Steel ZY&ITp." Ye. To. Chaburkova, Cm Bel Ron Inst of Technol and Jkch Cmetr,, 3 pp- ftwa& Lab" Vol XV, No. 3 MactrelytIc method in utilized for extractIM ammoullic Impurities from MIT austealte iumal. .Zlectrolytlc diffusim of austealts aftel "1d, be perf m d in a 6% solution or I'mulfate with addltlm of 0.2% sodims 7% wAlm, chloride to the eiectio2yte, USSR/Metals Cast Iron Jun-50 Chemistry - Magnesium, Determination "Determination of Magnesium in Cast Iron," Ye. 1-4 Ye. Cheburkova, Cen Sci Res inst of Tech and Mach Constr "Zavod Lab" Vol XVI, Wo 6, pp 663-666 Desertbes experiments to develop most efficient wthod for determination of magnesium in cast Irons Separation of iron performed with aid of other, and ammonia and bromine water used for sepax-atIng nan anese. T4o -possibilities investi- gmted for determination of magnesium im- presence ZOT54 USW/-*4etals cast iron Jun 50 (Coutd) of copper-~ b7droquinoline methocL, and analys is phoap~hate nethod. Latter method suggested as ,betteT- because it Is simpler, does not require preliminary separation of copper, and employs'no s~eetal reagents. USSR/Metals - Welding, Fluxes, Aug 50 Analysis *Determination of Fluorine in Welding Fluxes," Ye. Ye. Cheburkova, Cen Sci.Res Inst of Technol and Mach Bldg "Zavod Lab" Vol XVI, No 8y 1009-1010 Suggests accelerated method for determinatioz of P in welding fluxes - F is brought into olution in forid of Na F for which purpose lux. under investigation has to be sintered ; with mixture of 3 parts of ZnO and I part Na carbonate. At end of procedure precipitate 169r44 USSR/14etals - Welding, Fluxes, Aug 50 (Coutd) of Pb fluordbromide is obtained, and upon its reaction with Ag nitrate, content of F in flux may be calculated~be determination !,"of ..quantity of Ag nitrate.,combined with Br. 8 . (f Ye. Y6-- 137-58-2-4154 Translation from: Referativnyy zhurnal, Metallurgiya, 1958, Nr 2, p 270 (USSR) AUTHOR: Cheburkova, Ye.Ye. TITLE: The Nonmetallic Inclusions in an Austenitic CF rome -nickel -cobalt Steel Alloyed With Niobium (Nemetallicheskiye vklyucheniya v austenitnoy khromonikel'kobal'tovoy stali s niobiyem) PERIODICAL: V sb.. Fiz.-kbim. issled. austenitn. splavov. Moscow, Mashgiz, 1957, pp 41-52 ABSTRACT: An investigation was made of steel EI-434 relative to its nonmetallic inclusions. Employed was a new method of separating the carbides and nonmetallic inclusions by means of their differing solubility in acid oxidizing media. The residues were examined and the total quantity of nonmetallic inclusions determined by chemical analysis. The nature of the nonmetallic inclusions was determined by a microscopic investigation of the residues in diffracted light. Methods were devised for determining the non- metallic oxide inclusions in steel El-434. The total quantity, composition, and nature of the nonmetallic inclusions were ascertained, and it was noted that in steel EI-434 the predorni-' Card 1/2 nant nonmetallic inclusions, by and large, consisted of SiO 2' 13 7- 58-2-4154 The Nonmetallic Inclusions in an Austenitic Chrome -nickel -cobalt Steel (cont.) FeO, and Al 20 3 * Insignificant quantities of Cr203 and Nb 20 3 were found. Bibliography: 7 references. T. F. U 3t*91 allwa-Inci=iOns Card 2 /Z CHIBURKOVA, Ye.ye., kand.tekhnoneuk Nometallic inclusions In mustenitic chromium-nickel-cobalt steels. containing n1oblum. [Trudy] TSNIITKASH 84-41-52 '57 (MIRA 10:11) (Steel alloys-~Analysls) (Oxides) TXMIN, N.I., kand. fis. -MRt. nail ; TZWHIM' F.Ko' insh.; KOX&ROMIT. A.G., kand.tekhn.vAuk; CHBNIMVA, Te.Te., kand.tekhn.nauk; SMISY, B.A, . imnd.tilffiin~.nauk-.~~.. ., kzLnd.tekhn.n&uk PkWalcal and chemical "thods for the Investigation in the phase analysis of alloys. [Tmdg] TsNimm moo-W 159. (KIM 13:7) (Alloy@) BORZUNOV, S.K., polkovnikl CHEBUSHU. LV.. polkqynik. red.: VOLKOTA. T.Ye., tekhn.red. [Decrees of the October Plenum of the Central Committee of the CPSU In action] Pleshentia oktiabrlskogo Plenuma TaK KPSS v deistvit. Moskva, Toon.Lad-wo N-va obor.SSSRO 1959* 371 P. (KIRA 12:4) (Russia-Armed forces) LkRIKOV, A.M., polkovnik, kand.istor.nauk; FILIPPOV, N.T., polkoynik, kand. ytLridich.nauk; BOCHKAREV, X.S., general-mayor, dotsent, kand.filosol. nauk. red.; CH&BUSMff, 1J., polkovnik, red.; KAKOTEV, V.P., tekhn. red. [Unity of co=and In the Soviet Armed Forces and ways for further strengthening it; a lecture presented to the troops] Edinona- chalie v Sovetakikh Tooruzhannykh Silakh I puti ego dallneishego ukrepleniia; laktaila, prochitannais v voisicakh. Moskva, Voen. izd-va X-va obor.SSSR. 1960. 38 p. (KIU 13..6) 1. Lektory Glovnogo politicheskogo uprsvleniya Sovetskoy Irmii I Voyenno-Korskogo Flota (forlarlkov. 'Filippov). . (ftesis--Arsod forces--Officers) ZZWBOV. A.A., polkoynik; PADWN, Ym.A., polkovnik; CHOUSM, I.V., polkovnik, red.; NEMENA. A.N.. tekhn.red. -- Eftrty ormnisations in armW units and war vessels-, collected article@ on the work mperience of local party organizations] Partiinsia organizatelia chesti, korablia; abornik statel ob opyte raboty pervichnykh partorgamizateli. Moskva, Voen.lsd-vo X-va obor.S=. 1960. 334 p. (KIU 13:4) (Commmist Nrty of the Soviet Uhlon--Party work) (fteele-Armod forces) 9 LIPODAM, Ivan Alekseyevich, General-leytenant; CHEB . polkov- I - nik, red.; BUKOVSKAYA, N.A., tekbn. red. [Steadfastly endure the hardships and privations of military service] Stoiko perenosit' tiagoty i 3-ishaniia voemoi sluzhby. Moskva, Voen.izd-vo M-va obcrony SSSR 1961. 75 P. (KIRA 14:12) (Military education~