نتایج جستجو برای: cd tetraphenyl porphyrin

تعداد نتایج: 54552  

2007
Fengyang Wang Xueying Huang Li Du Weiguo Li Hongxuan He Chao Qi

The small molecule, meso-tetra(α,α,α,α-o-phenylacetamidophenyl)porphyrin (Mr1147.0) was used as complete antigen to elicit MAb through the immunization and cell fusion techniques.The MAb 1F2 obtained was demonstrated to be very pure by MALDI/TOFMS.The subtype of MAb 1F2 is IgG2a, which has a relative molecular weight of 156,678.8 Da.No significant change in the intensity of absorption peaks in ...

A PVC ion-selective membrane electrode based on Cd-tetraphenyl porphyrine as a carrier was prepared fordetermination of MnO4- ion. This electrode revealed good selectivity toward permanganate ion over a widevariety of anions. Effects of some experimental parameters such as nature of the plasticizer, the amounts ofcarrier and additive, and concentration of the internal solution on the potential ...

Journal: :Journal of the American Chemical Society 2001
T Kurtán N Nesnas Y Q Li X Huang K Nakanishi N Berova

A general microscale protocol for the determination of absolute configurations of primary amino groups or secondary hydroxyl groups linked to a single stereogenic center is described. The chiral substrates are linked to the achiral trifunctional bidentate carrier molecule (3-aminopropylamino)acetic acid (1, H(2)NCH(2)CH(2)CH(2)NHCH(2)COOH) and the resultant conjugates are then complexed with di...

Journal: :Chemical & pharmaceutical bulletin 2001
Y Ishikawa A Yamashita T Uno

Positively charged porphyrins bearing an acridine with various lengths of diamino alkyl linkage, 5-[4-[(6-chloro-2-methoxy-9-acridyl)aminoalkylaminocarbonyl]phenyl]-10,15,20-tris(4-N-methylpyridiniumyl)porphine triiodide, alkyl=ethyl, butyl, hexyl, or octyl, were synthesized. They exhibited more enhanced photocleavage activity of pUC18 plasmid DNA than TMPyP, meso-tetrakis(4-N-methylpyridiniumy...

Some meso-tetra aryl porphyrinato manganese (III) acetate or chloride complexes including meso-tetraphenyl porphyrinato manganese (III) chloride (TPPMnCl), meso-tetrakis(2,3-dimethoxyphenyl)porphyrinato manganese(III) acetate, (T(2,3-OMeP)PMnOAc) and meso-tetrakis(pentaflourophenyl)porphyrinato manganese (III) acetate (TPFPPMnOAc) were synthesized. These porphyrins were used as catalyst in the ...

A.F.B Mahdavi K. Zare M. Akbarzadeh M. Keshavarz M.R khoshchehreh

In the present work, the interaction of three water soluble porphyrins, tetra (p-trimethyle) ammoniumphenyl porphyrin iodide (TAPP) as a cationic porphyrin, tetra sodium meso-tetrakis (p-sulphonatophenyle) porphyrin (TSPP) as an anionic porphyrin and manganese tetrakis (p-sulphonato phenyl)porphinato acetate (MnTSPP) as a metal porphyrin, with DNA have been studied by isothermaltitration microc...

2013
Hamza Toumi Yassine Belghith Jean-Claude Daran Habib Nasri

The title compound, [Cd(C44H28N4)(H2O)]·(C12H24O6), was made by the reaction of the [Cd(TPP)] with an excess of 18-crown-6 in chloro-benzene (where TPP is tetra-phenyl-porphyrinate). The Cd(II) cation is chelated by a TPP anion and coordinated by a water mol-ecule in a distorted N4O square-pyramidal geometry, the Cd(II) cation being displaced by 0.7533 (9) Å from the mean plane of four N atoms ...

Journal: :Molecules 2011
Jang-Hwan Hong

The reductive cleavage of the Si-Si bond in 1,1-bis(1-methyl-2,3,4,5-tetraphenyl-1-silacyclopentadiene) [(C(4)Ph(4)SiMe)(2)] (1) with either Li or Na in THF gives the silole anion [MeSiC(4)Ph(4)]- (2). The head-to-tail dimerization of the silole anion 2 gives crystals of the disilatricyclic diallylic dianion [(C(4)Ph(4)SiMe)(2)]-2 (3). The derivatization of 3 (crystals) with bromoethane (gas) u...

Journal: :Chemical communications 2012
Hirokuni Jintoku Makoto Takafuji Reiko Oda Hirotaka Ihara

Enantioselective recognition of amino acids was achieved by using a highly ordered chiral assembly of achiral porphyrin on a chiral molecular gel. Exceptionally high enantioselectivity was observed for histidine derivatives by monitoring the CD patterns and fluorescence quenching, K(SV) (l): 26.3 × 10(3) M(-1); K(SV)(D)-enantiomer: 7.03 × 10(3) M(-1).

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