95 resultados para methyl 2

em Repositório Institucional UNESP - Universidade Estadual Paulista "Julio de Mesquita Filho"


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Molecular mobility in castor oil based polyurethane was investigated with thermally stimulated depolarization current (TSDC) measurements and alternating-current (ac) dielectric relaxation spectroscopy. Three peaks could be observed in TSDC thermograms from 173 to 373 K. The relaxation located at 213 K could be attributed to the change in the molecular chain due to the interaction between the isocyanate and the solvent, and it was well fitted with the Vogel-Fulcher-Tammann equation. The other two peaks were located at 274 and 365 K and could be attributed to interfacial polarization and space charge, respectively. (c) 2005 Wiley Periodicals, Inc.

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4-Methylpyrimidine-2-thione reacts with methylmercury hydroxide to give the thiolate derivative HgMe(SC4H2N2Me-2), the X-ray structure of which reveals pairs of molecules with a mercury-mercury distance of 3.10 Å.

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In the title compound, C12H15N3S, the mol­ecule deviates slightly from planarity, with a maximum deviation from the mean plane of the non-H atoms of 0.2756 (6) Å for the S atom and a torsion angle for the N-N-C-N fragment of -7.04 (16)°. In the crystal, mol­ecules are linked by N-H...S hydrogen-bond inter­actions, forming centrosymmetric dimers. Additionally, one weak intra­molecular N-H...N hydrogen-bond inter­action is observed. The crystal packing shows a herringbone arrangement viewed along the c axis.

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Objetivou-se neste trabalho avaliar a seletividade de herbicidas aplicados nas gramas Santo Agostinho (Stenotaphrum secundatum) e Esmeralda (Zoysia japonica) em condições de campo. O delineamento experimental utilizado foi o de blocos casualizados, com quatro repetições. As gramas foram cortadas a 3 cm de altura e, em seguida, foram feitas as aplicações dos herbicidas. Os tratamentos utilizados foram: testemunha sem aplicação, fluazifop-p-butil (125 g ha-1), sethoxydim+óleo mineral (276 g ha-1 + 0,5% v v-1 de Assist), bispyribac-sodium (25 g ha-1), chlorimuron-ethyl (15 g ha-1), ethoxysulfuron (150 g ha-1), halosulfuron (112,5 g ha-1), iodosulfuron-methyl (10 g ha-1), metsulfuron-methyl (2,4 g ha-1), nicosulfuron (125 g ha-1), pyrithiobac-sodium (140 g ha-1), trifloxysulfuron-sodium (22,5 g ha-1), 2,4-D (720 g ha-1), quinclorac (375 g ha-1), atrazina (1.250 g ha-1), bentazon (600 g ha-1), linuron (1.350 g ha-1), fomesafen (187,5 g ha-1), lactofen (120 g ha-1), oxadiazon (600 g ha-1) e oxyfluorfen (720 g ha-1). Os herbicidas que apresentaram potencial de seletividade para o gramado de S. secundatum foram: os inibidores da ALS chlorimuron-ethyl, ethoxysulfuron, halosulfuron, iodosulfuron-methyl e metsulfuron-methyl, o mimetizador de auxina 2,4-D, os inibidores do fotossistema II atrazina e bentazon, bem como os inibidores da Protox fomesafen, lactofen e o oxadiazon. Para o gramado de Z. japonica, os herbicidas que apresentaram potencial de seletividade foram: os inibidores da ALS chlorimuron-ethyl, ethoxysulfuron, halosulfuron, metsulfuron-methyl e nicosulfuron, os mimetizadores de auxina 2,4-D e quinclorac, os inibidores do fotossistema II atrazina e bentazon, além dos inibidores da Protox fomesafen, lactofen e o oxadiazon.

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Objetivou-se avaliar a seletividade de herbicidas aplicados na grama Batatais (Paspalum notatum) e na grama São Carlos (Axonopus compressus) em campo. O delineamento experimental utilizado foi o de blocos casualizados com quatro repetições. As gramas foram cortadas a 3 cm de altura e, em seguida, realizaram-se as aplicações dos herbicidas. Os tratamentos utilizados foram: testemunha (sem aplicação), fluazifop-p-butil (125 g ha-1), sethoxydim+óleo mineral (276 g ha-1 + 0,5% v v-1 de Assist), bispyribac-sodium (25 g ha-1), chlorimuron-ethyl (15 g ha-1), ethoxysulfuron (150 g ha-1), halosulfuron (112,5 g ha-1), iodosulfuron-methyl (10 g ha-1), metsulfuron-methyl (2,4 g ha-1), nicosulfuron (125 g ha-1), pyrithiobac-sodium (140 g ha-1), trifloxysulfuron-sodium (22,5 g ha-1), 2,4-D (720 g ha-1), quinclorac (375 g ha-1), atrazina (1.250 g ha-1), bentazon (600 g ha-1), linuron (1.350 g ha-1), fomesafen (187,5 g ha-1), lactofen (120 g ha-1), oxadiazon (600 g ha-1) e oxyfluorfen (720 g ha-1). Os herbicidas que apresentaram potencial de seletividade para o gramado de P. notatum foram o chlorimuron-ethyl, ethoxysulfuron, pyrithiobac-sodium, 2,4-D, bentazon e fomesafen; já para o gramado de A. compressus foram o chlorimuron-ethyl, ethoxysulfuron, halosulfuron, iodosulfuron-methyl, metsulfuron-methyl, pyrithiobac-sodium, 2,4-D, quinclorac, atrazina, bentazon, além do fomesafen.

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Blend films (free-standing) containing 20% in volume of polyaniline (PANI) in 80% of natural rubber (NR) were fabricated by casting in three different ways: (1) adding PANI-EB (emeraldine base) dissolved in N-methyl-2-pyrrolidone (NMP) to the latex (NRL), (2) adding PANI-EB dissolved in in-cresol to NR dissolved in xylol (NRD), (3) overlaying the surface of a pure NR cast film with a PANI layer grown by in situ polymerization (NRO). All the films were immersed into HCl solution to achieve the primary doping (protonation) of PANI before the characterization. The main goal here was to investigate the elastomeric and electrical conductivity properties for each blend, which may be applied as pressure and deformation sensors in the future. The characterization was carried out by optical microscopy, dc conductivity, vibrational spectroscopy (infrared absorption and Raman scattering), thermogravimetry analysis (TGA), differential scanning calorimetry (DSC), dynamic mechanical thermal analysis (DMTA), and tensile stress-strain curves. The results suggest that the NRL blend is the most suitable in terms of mechanical and electrical properties required for applications in pressure and deformation sensors: a gain of conductivity without losing the elastomeric property of the rubber. (c) 2005 Wiley Periodicals, Inc.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

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The resolution of the natural racemic chromane 3,4-dihydro-5-hydroxy-2,7-dimethyl-8-(3 ''-methyl-2 ''-butenyl)-2-(4'-methyl-1',3'-pentadienyl)-2H-1-benzopyran-6-carboxylic acid (1) isolated from the leaves of Peperomia obtusifolia has been accomplished using stereoselective HPLC. The absolute coil figuration of the resolved enantiomers was determined by the analysis of optical rotations and CD spectra. The finding of a racemic mixture instead of an enantiomerically pure metabolite raises questions about the final steps in the biosynthesis of this class of natural products, suggesting that the intramolecular chromane ring formation step may not be enzymatically controlled at all in P. obtusifolia. Chirality 21:799-801, 2009. (C) 2008 Wiley-Liss, Inc.

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