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anisole/dental caries

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ČlankiKliničnih preskušanjPatenti
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Photophysical processes involved within the anisole-thioindoxyl dyad system.

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The photophysical properties and the nature of the photoinduced electron transfer (PET) reactions within a synthesized anisole (A)-thioindoxyl (T) dyad system (24MBTO) have been studied by electrochemical, steady-state, and time-resolved spectroscopic techniques. Computations on the dyad were

Peptide mimics by linear arylamides: a structural and functional diversity test.

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Hydrogen-bonded oligoamide foldamers represent a large family of peptide mimics. Pioneered by Gellman and Seebach (Appella , J. Am. Chem. Soc. 1996, 118, 13071- 13072; Seebach , Helv. Chim. Acta 1996, 79, 913- 941), aliphatic amino acid-based mimic structures have been extensively studied. Results

Structural requirements of para-alkylphenols to bind to estrogen receptor.

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Octyl- and nonylphenols in the environment have been proposed to function as estrogens. To gain insight into their structural essentials in binding to the estrogen receptor, a series of phenols with saturated alkyl groups at the para position, HO-C6H4-CnH2n+1 (n = 0-12), were examined for their

Metallocyclic receptors with Re(I)/Os(II)-based moieties: molecular photophysics and selective molecular sensing.

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New metallocyclic Re(I) and Os(II) complexes with polyphosphane/polyyne spacers, including dimers [(Re(CO)3Cl(C2nP2))2] (n = 1, 1; 2, 2) and tetramers [(Re(CO)3Cl(C2nP2))4] (n = 1, 3; 2, 4, C2P2 = Ph2P-C...C-PPh2, C4P2 = Ph2P-C...C-C...C-PPh2), as well as the mixed-metal

Spectral characteristics of tramadol in different solvents and beta-cyclodextrin.

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Effect of solvents and beta-cyclodextrin on the absorption and fluorescence spectra of tramadol drug has been investigated and compared with anisole. The solid inclusion complex of tramadol with beta-CD is investigated by FT-IR, (1)H NMR, scanning electron microscope (SEM), DSC and semiempirical
Since the flexible host framework of perfluorinated mononuclear copper complex, [Cu(L1)2] (1, HL1 = 3-hydroxy-1,3-bis(pentafluorophenyl)-2-propen-1-one), with CuO4 core reversibly encapsulated several organic guest molecules through electrostatic interactions in their crystals, the corresponding
BACKGROUND Stachybotrys chartarum is a filamentous mold frequently identified among the mycobiota of water-damaged building materials. Growth of S. chartarum on suitable substrates and under favorable environmental conditions leads to the production of secondary metabolites such as mycotoxins and

Thermodynamics of host-guest interactions between fullerenes and a buckycatcher.

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(1)H NMR and isothermal titration calorimetry (ITC) experiments were employed to obtain reliable thermodynamic data for the formation of the 1:1 inclusion complexes of fullerenes C(60) and C(70) with the buckycatcher (C(60)H(28)). NMR measurements were done in toluene-d8 and chlorobenzene-d5 at 288,
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