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  2. Chemistry Letters - Wikipedia

    en.wikipedia.org/wiki/Chemistry_Letters

    Chemistry Letters is a peer-reviewed scientific journal published by the Chemical Society of Japan. It specializes in the rapid publication of reviews and letters on all areas of chemistry. The editor-in-chief is Mitsuhiko Shionoya (University of Tokyo). According to the Journal Citation Reports, the journal has a 2014 impact factor of 1.23. [1]

  3. Supramolecular polymer - Wikipedia

    en.wikipedia.org/wiki/Supramolecular_polymer

    issn 0366-7022. Yano K, Itoh Y, Araoka F, Watanabe G, Hikima T, Aida T (January 2019). "Nematic-to-columnar mesophase transition by in situ supramolecular polymerization" .

  4. Mukaiyama hydration - Wikipedia

    en.wikipedia.org/wiki/Mukaiyama_hydration

    A recent review by Shenvi and coworkers, [8] proposed that the Mukaiyama hydration operates via the same principles as metal hydride hydrogen atom transfer (MH HAT), elucidated by Jack Halpern and Jack R. Norton in their studies on hydrogenation of anthracenes by syngas and Co 2 (CO) 8 [9] and the chemistry of vitamin B 12 mimics, [10 ...

  5. M-MTDATA - Wikipedia

    en.wikipedia.org/wiki/M-MTDATA

    m-MTDATA - whose full name is 4,4',4"-Tris(N-3-methylphenyl-N-phenyl-amino) triphenylamine - is an organic molecule belonging to the class of starburst molecules, [3] often used as a material for the production of organic electronic devices.

  6. Theodore Kuwana - Wikipedia

    en.wikipedia.org/wiki/Theodore_Kuwana

    Theodore Kuwana (1931–2022) was a chemist and academic researcher known as the founding father of the field of spectroelectrochemistry.. Kuwana's academic career included appointments at California Institute of Technology, the University of California, Riverside, Case Institute of Technology, Ohio State University, and finally at the University of Kansas.

  7. Murai reaction - Wikipedia

    en.wikipedia.org/wiki/Murai_reaction

    In organic chemistry, the Murai reaction is an organic reaction that uses C-H activation to create a new C-C bond between a terminal or strained internal alkene and an aromatic compound using a ruthenium catalyst. [1] The reaction, named after Shinji Murai, was first reported in 1993.

  8. AOL Mail

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    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  9. Tellurophenes - Wikipedia

    en.wikipedia.org/wiki/Tellurophenes

    The C-C bond length was observed to be 1.326(4) Å, much longer than a C-C triple bond and closer to a C-C double bond, indicating that the compound had activated phenylacetylene through FLP chemistry.