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The highest percentage conversion was obtained using a 1∶1 mole ratio of alcohol to ferulic acid in stirred batch reactions in anhydrous 2-methyl-2-propanol at 60°C using one equivalent (wt/wt based on ferulic acid) of Novozym 435.
      
The reduction reaction proceeds in a homogeneous medium under mild conditions, one equivalent of the reducing agent being consumed per each quinoid carbonyl.
      
The radical cation underwent a second one-electron oxidation to form a brownish yellow coloured dication [DBCP2+] in the presence of more than one equivalent of cerium(IV), which was characterized by UV-vis, IR and mass spectrometry.
      
6 a, b can be cyclized with one equivalent of aqueous hydrogen bromide to9 a, b.
      
Methyl 6-O-(tBDMSi)-β-D-galactopyranoside (1 a) and methyl 6-O-(tBDMSi)-α-D-mannopyranoside (6 a) can be prepared from1 or6 with one equivalent oft-butyldimethylchlorosilane.
      
2,3,4-Trichlorothiophene undergoes metal-hydrogen exchange with one equivalent of butyllithium inTHF at -78°C to give trichloro-2-thienyllithium in 91% yield.
      
Similar treatment of (C5Me5)2 Ce(μ-Cl)2K(THF)2 with one equivalent of1 affords the neutral species (C5Me5)Ce(FcN)Cl (6)via displacement of one C5Me5 ligand.
      
Bisphophinite complexes of Pd (II) are shown to be ideal and they work best in the presence of one equivalent of water.
      
saccharobutyricum shows that the primary action is produced upon a first substance X, very likely an enzyme, following a mechanism such as one equivalent of oxygen gives a reversible combination, and two equivalents an irreversible combination.
      
In this survey, a new minimax inequality and one equivalent geometricform are proved.
      
Since V2O5 has only one equivalent cation site, it is concluded that this efg belongs to111Cd at this site.
      
The relative inclusion selectivity of a series of 21 terpene and aromatic guest molecules with regard to β-CD have been measured in an aqueous environment, based on the interaction of 1∶1 mixtures of the guest molecule with one equivalent of β-CD.
      
While a deductive system can have at most one equivalent algebraic semantics, it may have numerous different algebraic semantics.
      
The reactions of [MI2(CO)3(NCMe)2] (M=Mo or W) with one equivalent of L(L-phosphorus, arsenic and antimony donor ligands) to aff
      
The dicationic mixed ligand complexes [M(CO)3(bipy)(5,6-Me2-phen)]2I (22 and23) are prepared by reacting [MI2(CO)3(NCMe)2] with one equivalent of bipy, followed by anin situ reaction with 5,6-Me2-1, 10-phen to afford the products22 and23.
      
Quantitative transport of one equivalent of M2+ from the aqueous to the organic (CH2Cl2) phase can be achieved with two equivalents of [OsA3]-.
      
The platinum complexes [PtMe2(dpmMe)] or [Pt(CH2)4(dpmMe)] fail to undergo ring-opening on treatment with one equivalent of dpmMe [dpmMe = Ph2PCH(Me)PPh2].
      
The first stage is a one equivalent outer sphere electron transfer to form [Fe2- (CN)10]5- and the radical cation tu+· which dimerises to form the disulfide tu22+.
      
This mixed-ligand complex is oxidized in two steps, each involving one equivalent of charge per complex present, as indicated by controlled-potential electrolyses done at +0.30V versus s.c.e.
      
In the presence of hydriodic acid, one equivalent of acid is included in the complex.
      
 

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