نتایج جستجو برای: chiral stability

تعداد نتایج: 336584  

Journal: :journal of physical & theoretical chemistry 2004
issa yavari vahideh hadigheh-rezvan mohsen dadgar

ab initio calculations at hf/6-31g* level of theory for geometry optimization and mp2/6-31g*//hf/6-31g* for a single point total energy calculation are reported for the importantenergy-minimum conformations and transition-state geometries of 1, 3-diazacyclohepta-1, 2-diene (2) and 1, 3-diazacycloocta-1, 2-diene (3). the c2 symmetric twist-chair (2-tc)conformation of 2 is calculated to be 7.4 kj...

Journal: :international journal of bio-inorganic hybrid nanomaterials 0

an efficient one-pot three-component procedure for the synthesis of new chiral spiro-oxindolopyrrolizidines with highly regio-, diastereo-, and enantioselective from 1,3-dipolar cycloaddition of azomethine ylides and optically pure active cinamoyl oxazolidinone are described. the process occurs at room temperature in aqueous ethanol as green solvent and in the absence of any bidentate chelating...

Journal: :Journal of Functional Analysis 2018

Journal: :journal of the iranian chemical research 0
jahanbaksh ghasemi department of chemistry, faculty of sciences, k.n. toosi university of technology, tehran, iran mahmood chamsaz department of chemistry, faculty of sciences, ferdowsi university of mashhad, iran saeid asadpour department of chemistry, faculty of sciences, ferdowsi university of mashhad, iran ali sarafraz yazdi department of chemistry, faculty of sciences, ferdowsi university of mashhad, iran

in recent years there has been considerable interest in the synthesis and separation of enantiomers of organic compounds especially because of their importance in the biochemistry and pharmaceutical industry. high-performance liquid chromatography is a very useful method for the direct separation of enantiomers. however, about 30−40 years ago, commercially available chiral stationary phases wer...

Ali Sarafraz Yazdi Jahanbaksh Ghasemi, Mahmood Chamsaz Saeid Asadpour

In recent years there has been considerable interest in the synthesis and separation of enantiomers of organic compounds especially because of their importance in the biochemistry and pharmaceutical industry. High-performance liquid Chromatography is a very useful method for the direct separation of enantiomers. However, about 30−40 years ago, commercially available chiral stationary phases wer...

Journal: :the iranian journal of pharmaceutical research 0
farrin sattary javid pharmaceutical chemistry department, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. alireza shafaati pharmaceutical chemistry department, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. afshin zarghi pharmaceutical chemistry department, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran.

one of the problems encountered in ce separations of basic compounds is the adsorption of analytes onto the negatively charged capillary wall which could lead to poor repeatability of migration time and peak area. additionally, separation of enantiomers of chiral of basic drugs is commonly carried out in low ph buffer which contributes to strong ionic interaction of the cationic drug ions with ...

2013
Harold STEINACKER Jochen ZAHN

We introduce an index indicating the occurrence of chiral fermions at the intersection of branes in matrix models. This allows to discuss the stability of chiral fermions under perturbations of the branes.

Journal: :Physical review letters 2011
T Aaltonen B Álvarez González S Amerio D Amidei A Anastassov A Annovi J Antos G Apollinari J A Appel A Apresyan T Arisawa A Artikov J Asaadi W Ashmanskas B Auerbach A Aurisano F Azfar W Badgett A Barbaro-Galtieri V E Barnes B A Barnett P Barria P Bartos M Bauce G Bauer F Bedeschi D Beecher S Behari G Bellettini J Bellinger D Benjamin A Beretvas A Bhatti M Binkley D Bisello I Bizjak K R Bland B Blumenfeld A Bocci A Bodek D Bortoletto J Boudreau A Boveia B Brau L Brigliadori A Brisuda C Bromberg E Brucken M Bucciantonio J Budagov H S Budd S Budd K Burkett G Busetto P Bussey A Buzatu C Calancha S Camarda M Campanelli M Campbell F Canelli A Canepa B Carls D Carlsmith R Carosi S Carrillo S Carron B Casal M Casarsa A Castro P Catastini D Cauz V Cavaliere M Cavalli-Sforza A Cerri L Cerrito Y C Chen M Chertok G Chiarelli G Chlachidze F Chlebana K Cho D Chokheli J P Chou W H Chung Y S Chung C I Ciobanu M A Ciocci A Clark G Compostella M E Convery J Conway M Corbo M Cordelli C A Cox D J Cox F Crescioli C Cuenca Almenar J Cuevas R Culbertson D Dagenhart N d'Ascenzo M Datta P de Barbaro S De Cecco G De Lorenzo M Dell'Orso C Deluca L Demortier J Deng M Deninno F Devoto M d'Errico A Di Canto B Di Ruzza J R Dittmann M D'Onofrio S Donati P Dong M Dorigo T Dorigo K Ebina A Elagin A Eppig R Erbacher D Errede S Errede N Ershaidat R Eusebi H C Fang S Farrington M Feindt J P Fernandez C Ferrazza R Field G Flanagan R Forrest M J Frank M Franklin J C Freeman Y Funakoshi I Furic M Gallinaro J Galyardt J E Garcia A F Garfinkel P Garosi H Gerberich E Gerchtein S Giagu V Giakoumopoulou P Giannetti K Gibson C M Ginsburg N Giokaris P Giromini M Giunta G Giurgiu V Glagolev D Glenzinski M Gold D Goldin N Goldschmidt A Golossanov G Gomez G Gomez-Ceballos M Goncharov O González I Gorelov A T Goshaw K Goulianos A Gresele S Grinstein C Grosso-Pilcher R C Group J Guimaraes da Costa Z Gunay-Unalan C Haber S R Hahn E Halkiadakis A Hamaguchi J Y Han F Happacher K Hara D Hare M Hare R F Harr K Hatakeyama C Hays M Heck J Heinrich M Herndon S Hewamanage D Hidas A Hocker W Hopkins D Horn S Hou R E Hughes M Hurwitz U Husemann N Hussain M Hussein J Huston G Introzzi M Iori A Ivanov E James D Jang B Jayatilaka E J Jeon M K Jha S Jindariani W Johnson M Jones K K Joo S Y Jun T R Junk T Kamon P E Karchin Y Kato W Ketchum J Keung V Khotilovich B Kilminster D H Kim H S Kim H W Kim J E Kim M J Kim S B Kim S H Kim Y K Kim N Kimura M Kirby S Klimenko K Kondo D J Kong J Konigsberg A V Kotwal M Kreps J Kroll D Krop N Krumnack M Kruse V Krutelyov T Kuhr M Kurata S Kwang A T Laasanen S Lami S Lammel M Lancaster R L Lander K Lannon A Lath G Latino I Lazzizzera T LeCompte E Lee H S Lee J S Lee S W Lee S Leo S Leone J D Lewis C-J Lin J Linacre M Lindgren E Lipeles A Lister D O Litvintsev C Liu Q Liu T Liu S Lockwitz N S Lockyer A Loginov D Lucchesi J Lueck P Lujan P Lukens G Lungu J Lys R Lysak R Madrak K Maeshima K Makhoul P Maksimovic S Malik G Manca A Manousakis-Katsikakis F Margaroli C Marino M Martínez R Martínez-Ballarín P Mastrandrea M Mathis M E Mattson P Mazzanti K S McFarland P McIntyre R McNulty A Mehta P Mehtala A Menzione C Mesropian T Miao D Mietlicki A Mitra H Miyake S Moed N Moggi M N Mondragon C S Moon R Moore M J Morello J Morlock P Movilla Fernandez A Mukherjee Th Muller P Murat M Mussini J Nachtman Y Nagai J Naganoma I Nakano A Napier J Nett C Neu M S Neubauer J Nielsen L Nodulman O Norniella E Nurse L Oakes S H Oh Y D Oh I Oksuzian T Okusawa R Orava L Ortolan S Pagan Griso C Pagliarone E Palencia V Papadimitriou A A Paramonov J Patrick G Pauletta M Paulini C Paus D E Pellett A Penzo T J Phillips G Piacentino E Pianori J Pilot K Pitts C Plager L Pondrom K Potamianos O Poukhov F Prokoshin A Pronko F Ptohos E Pueschel G Punzi J Pursley A Rahaman V Ramakrishnan N Ranjan I Redondo P Renton M Rescigno F Rimondi L Ristori A Robson T Rodrigo T Rodriguez E Rogers S Rolli R Roser M Rossi F Rubbo F Ruffini A Ruiz J Russ V Rusu A Safonov W K Sakumoto Y Sakurai L Santi L Sartori K Sato V Saveliev A Savoy-Navarro P Schlabach A Schmidt E E Schmidt M P Schmidt M Schmitt T Schwarz L Scodellaro A Scribano F Scuri A Sedov S Seidel Y Seiya A Semenov F Sforza A Sfyrla S Z Shalhout T Shears P F Shepard M Shimojima S Shiraishi M Shochet I Shreyber A Simonenko P Sinervo A Sissakian K Sliwa J R Smith F D Snider A Soha S Somalwar V Sorin P Squillacioti M Stancari M Stanitzki R St Denis B Stelzer O Stelzer-Chilton D Stentz J Strologas G L Strycker Y Sudo A Sukhanov I Suslov K Takemasa Y Takeuchi J Tang M Tecchio P K Teng J Thom J Thome G A Thompson E Thomson P Ttito-Guzmán S Tkaczyk D Toback S Tokar K Tollefson T Tomura D Tonelli S Torre D Torretta P Totaro M Trovato Y Tu F Ukegawa S Uozumi A Varganov F Vázquez G Velev C Vellidis M Vidal I Vila R Vilar J Vizán M Vogel G Volpi P Wagner R L Wagner T Wakisaka R Wallny S M Wang A Warburton D Waters M Weinberger W C Wester B Whitehouse D Whiteson A B Wicklund E Wicklund S Wilbur F Wick H H Williams J S Wilson P Wilson B L Winer P Wittich S Wolbers H Wolfe T Wright X Wu Z Wu K Yamamoto J Yamaoka T Yang

We report the most sensitive direct search for pair production of fourth-generation bottomlike chiral quarks (b') each decaying promptly to tW. We search for an excess of events with an electron or muon, at least five jets (one identified as due to a b or c quark), and an imbalance of transverse momentum by using data from pp collisions collected by the CDF II detector at Fermilab with an integ...

2006
R. J. Baxter

It has been known for some time that the Boltzmann weights of the chiral Potts model can be parametrized in terms of hyperelliptic functions, but as yet no such parametrization has been applied to the partition and correlation functions. Here we show that for N = 3 the function S(t p) that occurs in the recent calculation of the order parameters can be expressed quite simply in terms of such a ...

Journal: :physical chemistry research 0
samira peymani ferdowsi university of mashhad mohammad izadyar ferdowsi university of mashhad ali nakhaeipour ferdowsi university of mashhad

in this study, kinetics and mechanism of the sulfur dioxide adsorption on the single-walled carbon nanotubes (cnt) are investigated. three single-walled carbon nanotubes, including the armchair (6,6), chiral (6,5) and zigzag (6,0) cnts were chosen as the models and the different orientations of so2 molecule relative to the cnt axis were considered. the b3lyp functional within the 6-31g(d) basis...

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