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Chromophoric block

Elimination of the 12a-OH function would extend the chromophore (by producing an additional DB at 12a-l) and eliminate activity. Substituting a halogen into position 11a would constitute a chromophoric block. Both of the preceding actions would predictably result in considerably decreased activity. [Pg.245]

The triazinyl ring acts as a chromophoric block, isolating the A/Q chromogen from the azo system and resulting in a clear green by a simple... [Pg.89]

Miscellaneous Disazo Dyes. Another group of disazo dyes is prepared by condensation of two identical or different aminoazo compounds commonly with phosgene, cyanuric chloride, or fumaryl dichloride, the fragments of which act as blocking groups between chromophores. [Pg.431]

In this way, many green azo dyes have been made by combining separate conjugated systems in the same molecule, eg, one yellow and the other blue. The blocking or the insulating group prevents the electronic interaction of one chromophore system with the second. Chloramine Fast Scarlet 4BS... [Pg.432]

We have studied two types of polymers that both belong to the second case those in which luminescent chromophores (typically K-coujugatcd oligomers) are separated by higher-energy-gap blocks (see Fig. 16-1 a) and those in which the chromophores are linked to each other in a non-coplanar way (sec Fig. 16-lb). [Pg.294]

Nanoscale Morphological Change of PS-b-P4VP Block Copolymer Films Induced by Site-Selective Doping of a Photoactive Chromophore... [Pg.208]

Direct and indirect competition formats, illustrated in Figure 1, are widely used for both qualitative and quantitative immunoassays. Direct competition immunoassays employ wells, tubes, beads, or membranes (supports) on to which antibodies have been coated and in which proteins such as bovine semm albumin, fish gelatin, or powdered milk have blocked nonspecific binding sites. Solutions containing analyte (test solution) and an analyte-enzyme conjugate are added, and the analyte and antibody are allowed to compete for the antibody binding sites. The system is washed, and enzyme substrates that are converted to a chromophore or fluorophore by the enzyme-tracer complex are added. Subsequent color or fluorescence development is inversely proportionate to the analyte concentration in the test solution. For this assay format, the proper orientation of the coated antibody is important, and anti-host IgG or protein A or protein G has been utilized to orient the antibody. Immunoassays developed for commercial purposes generally employ direct competition formats because of their simplicity and short assay times. The price for simplicity and short assay time is more complex development needed for a satisfactory incorporation of the label into the antibody or analyte without loss of sensitivity. [Pg.681]

The optical and electrochemical properties of porphyrins make these chromophores useful building blocks for the synthesis of electro- and photoactive polymers. Two types of linear polymers have been constructed using the self-assembly approach homo-polymeric assemblies and hetero- or shish kebab polymers. [Pg.249]

Dendritic molecules with electroactive units at either the focal point or core have been reported [92, 97]. There are, however, only a few examples of such moieties specifically pinned within cascade infrastructure. Our recent efforts in this direction [104-106] involve the incorporation of chromophoric 1,4-di-aminoanthraquinone (35) within the cascade infrastructure. Dendrimers based on a four-directional pentaerythritol core were synthesized using the extended 1 — 3 building block 36. A high dilution technique was applied to synthesize 36... [Pg.50]

Model analogs of the green type chromophore HBI have been chemically synthe-tized in different forms carrying blocking groups in place of the protein polypeptide chain [21, 24, 68, 69]. However, the covalent structure of HBI does not uniquely define its optical properties, because the molecule undergoes several protonation and conformational equilibria that directly affect its electronic structure. [Pg.353]

Figure 12.12 Building blocks of an artificial photosynthesis system for hydrogen production using a chromophore (C), an electron acceptor (A) and a sacrificial donor(D)... Figure 12.12 Building blocks of an artificial photosynthesis system for hydrogen production using a chromophore (C), an electron acceptor (A) and a sacrificial donor(D)...
If covalent bond formation occurs like for protonation, the ICT is blocked. However, due to the fact that stilbenes, coumarins and related chromophores with a weak or absent ICT character are commonly only weakly or nonfluorescent, the analyte-bound form would show strongly blue-shifted absorption spectra and virtually no emission, both undesirable features in terms of sensing. [Pg.47]

For some examples, see e.g. (a) Hogan CF, Harris AR, Bond AM et al (2006) Electrochemical studies of porphyrin-appended dendrimers. PhysChemChemPhys 8 2058-2065 (b) Jang W-D, Nishiyama N, Zhang G-D et al (2005) Supramolecular nanocarrier of anionic dendrimer porphyrins with cationic block copolymers modified with polyethylene glycol to enhance intracellular photodynamic efficacy. Angew Chem Int Ed 44 419 -23 (c) Loiseau F, Campagna S, Hameurlaine A et al (2005) Dendrimers made of porphyrin cores and carbazole chromophores as peripheral units. Absorption spectra, luminescence properties, and oxidation... [Pg.281]

Vincovalicine (30), C4(,H54N40,o, was isolated from C. ovalis (62) and exhibited a UV spectrum characteristic for the superposition of indole and indolenine chromophores, (log e) 220 (4.52), 256 (4.11), and 300 (3.99) nm. H-NMR data verified that a similar N-demethyl-N-formyl-vin-doline building block is present in 30 as in vincristine (2). Based on available data from the mass, UV, and H-NMR spectra structure 30 was suggested for vincovalicine, but this may need refinement. [Pg.33]


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See also in sourсe #XX -- [ Pg.89 ]




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