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  2. Organobismuth radical - Wikipedia

    en.wikipedia.org/wiki/Organobismuth_radical

    The first organopnictogen compound with a +2 oxidation state was the dicacodyl, tetramethyldiarsine ((CH 3) 2 As–As(CH 3) 2), reported in 1757. [7] However, heavier elements like Sb(II) and Bi(II) compounds were much harder to synthesize due to their high reactivity and tendency to progress via disproportionation reactions into their +3 and 0 oxidation states.

  3. Radical (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Radical_(chemistry)

    Lewis dot structure of a Hydroxide ion compared to a hydroxyl radical. In chemistry, a radical, also known as a free radical, is an atom, molecule, or ion that has at least one unpaired valence electron. [1] [2] With some exceptions, these unpaired electrons make radicals highly chemically reactive. Many radicals spontaneously dimerize. Most ...

  4. Stable phosphorus radicals - Wikipedia

    en.wikipedia.org/wiki/Stable_phosphorus_radicals

    Schematic of DFT calculation results for diphosphine radical 1 in the solid state, the syn,anti-• PR 2 radical (1A 2 and 1A 2), the H optimised radical (1B 1 and 1B 2), the syn,anti-• PR 2 radical fully optimised (1C), and syn,syn-• PR 2 radical in optimised geometry 2. Energies are in kJ mol −1. [13] Illustrating the "Jack-in-the-box ...

  5. Chemical species - Wikipedia

    en.wikipedia.org/wiki/Chemical_species

    The chemical species can be an atom, molecule, ion, or radical, with a specific chemical name and chemical formula. [ 2 ] In supramolecular chemistry , chemical species are structures created by forming or breaking bonds between molecules, such as hydrogen bonding , dipole-dipole bonds , etc. [ 3 ] These types of bonds can determine the ...

  6. Category:Free radicals - Wikipedia

    en.wikipedia.org/wiki/Category:Free_radicals

    العربية; Беларуская (тарашкевіца) Bosanski; Čeština; Deutsch; Ελληνικά; Español; Esperanto; فارسی; Français; Galego

  7. Radical initiator - Wikipedia

    en.wikipedia.org/wiki/Radical_initiator

    Benzoyl peroxide ((PhC)OO) 2) generates benzoyloxyl radicals (PhCOO•), each of which loses carbon dioxide to be converted into a phenyl radical (Ph•). Methyl ethyl ketone peroxide is also common, and acetone peroxide is on rare occasions used as a radical initiator, too. Inorganic peroxides function analogously to organic peroxides.

  8. 50 Adorable Memes That Prove Dogs Are From A Whole Other Planet

    www.aol.com/106-adorable-memes-dog-owners...

    They went from being wild animals to becoming man’s best friend. And some people even believe we don’t actually deserve them. Dogs have developed a well-deserved reputation as being loyal ...

  9. Conjugated system - Wikipedia

    en.wikipedia.org/wiki/Conjugated_system

    Cinnamaldehyde is a naturally-occurring compound that has a conjugated system penta-1,3-diene is a molecule with a conjugated system Diazomethane conjugated pi-system. In theoretical chemistry, a conjugated system is a system of connected p-orbitals with delocalized electrons in a molecule, which in general lowers the overall energy of the molecule and increases stability.

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