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  2. Cyclooctadiene iridium methoxide dimer - Wikipedia

    en.wikipedia.org/wiki/Cyclooctadiene_iridium_m...

    Cyclooctadiene iridium methoxide dimer is an organoiridium compound with the formula Ir 2 (OCH 3) 2 (C 8 H 12) 2, where C 8 H 12 is the diene 1,5-cyclooctadiene. It is a yellow solid that is soluble in organic solvents. The complex is used as a precursor to other iridium complexes, some of which are used in homogeneous catalysis. [1]

  3. Carbon-13 nuclear magnetic resonance - Wikipedia

    en.wikipedia.org/wiki/Carbon-13_nuclear_magnetic...

    The range for one-bond 1 J(13 C, 13 C) is 50–130 Hz. Two-bond 2 J(13 C, 13 C) are near 10 Hz. The trends in J(1 H, 13 C) and J(13 C, 13 C) are similar, except that J(1 H, 13 C are smaller owing to the modest value of the 13 C nuclear magnetic moment. Values for 1 J(1 H, 13 C) range from 125 to 250 Hz. Values for 2 J(1 H, 13 C) are near 5 Hz ...

  4. Triple-resonance nuclear magnetic resonance spectroscopy

    en.wikipedia.org/wiki/Triple-resonance_nuclear...

    Triple resonance experiments are a set of multi-dimensional nuclear magnetic resonance spectroscopy (NMR) experiments that link three types of atomic nuclei, most typically consisting of 1 H, 15 N and 13 C. These experiments are often used to assign specific resonance signals to specific atoms in an isotopically-enriched protein.

  5. Proton nuclear magnetic resonance - Wikipedia

    en.wikipedia.org/wiki/Proton_nuclear_magnetic...

    Proton nuclear magnetic resonance (proton NMR, hydrogen-1 NMR, or 1 H NMR) is the application of nuclear magnetic resonance in NMR spectroscopy with respect to hydrogen-1 nuclei within the molecules of a substance, in order to determine the structure of its molecules. [1]

  6. Infrared spectroscopy correlation table - Wikipedia

    en.wikipedia.org/wiki/Infrared_spectroscopy...

    1,1-disub. alkenes 1655 medium cis-1,2-disub. alkenes 1660 medium trans-1,2-disub. alkenes 1675 medium trisub., tetrasub. alkenes 1670 weak conjugated C═C dienes 1600 strong 1650 strong with benzene ring 1625 strong with C═O 1600 strong C═C (both sp 2) any 1640–1680 medium aromatic C═C any 1450 weak to strong (usually 3 or 4) 1500 1580

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  9. Dimethyl ether - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_ether

    As well as winning they beat the old standing record of 306 km/liter (326.8 cm 3 /100 km), set by the same team in 2007. [ 27 ] To study the dimethyl ether for the combustion process a chemical kinetic mechanism [ 28 ] is required which can be used for Computational fluid dynamics calculation.

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