Song Lin (chemist)

Last updated
Song Lin
Alma mater Harvard University
Peking University
Scientific career
Institutions Cornell University
University of California, Berkeley
Thesis Elucidation of the Cation-π Interaction in Small-Molecule Asymmetric Catalysis  (2013)
Doctoral advisor Eric Jacobsen
Other academic advisors Christopher Chang (post-doctoral advisor)
Website https://songlin.chem.cornell.edu/

Song Lin is a Chinese-American organic electrochemist who is an associate professor at Cornell University. His research involves the development of new synthetic organic methodologies that utilize electrochemistry to forge new chemical bonds. He is an Associate Editor of the journal Organic Letters, [1] and serves on the Early Career Advisory Board of Chemistry - A European Journal. [2] He was named by Chemical & Engineering News as one of their Trailblazers of 2022, a feature highlighting LGBTQ+ chemists in academia. [3] [4]

Contents

Early life and education

Lin was born in Tianjin. [3] He became interested in science as a child, doing simple household experiments, and was supported by his high school chemistry teacher to pursue a career in research. He completed his bachelor's degree in chemistry at Peking University where he worked under the supervision of Zhangjie Shi. [3] Lin moved to the United States for graduate studies and joined the organic chemistry department at Harvard University for doctoral research, where he researched small molecule asymmetric catalysis with Eric Jacobsen. [5] [6]

Research and career

Lin moved to the University of California, Berkeley for his postdoctoral research, where he worked in the lab of Christopher Chang. [3] [7] While studying electrocatalysis in Chang's lab, he became aware of the use of porous materials like covalent organic frameworks (COFs) to absorb carbon dioxide. [8] In collaboration with the Yaghi group, Lin showed that porphyrin-containing COFs could catalyze the electrocatalytic reduction of CO2 to CO under applied current and in an aqueous environment. [9] [10]

Lin began his independent career at Cornell University where his group's research has focused on the identification of novel synthetic pathways for medicinally relevant compounds. [11] He focuses on the use of electrochemistry to drive chemical reactions. [12] Electrochemistry can make organic synthesis cheaper and more environmentally friendly. For example, Lin demonstrated an electrochemical approach to synthesize 1,2-diamines from alkenes, which are useful precursors to bioactive natural products, therapeutic agents, and molecular catalysts. [13] [14] More recently, Lin's group has developed a method to directly couple alkyl halides using electrochemistry, providing a promising approach towards this difficult chemical transformation. [15] [16]

Awards and honors

Selected publications

Related Research Articles

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References

  1. "Editorial Board". pubs.acs.org. Retrieved 2022-05-26.
  2. Ross, Haymo (2021-01-04). "Chemistry: A European Journal and Chemistry Europe". Chemistry – A European Journal. 27 (1): 6–8. doi: 10.1002/chem.202005084 . ISSN   0947-6539. PMID   33393698. S2CID   230488554.
  3. 1 2 3 4 Joseph, Alby, J. (April 8, 2022). "One on One with Song Lin". cen.acs.org. Retrieved 2022-04-09.{{cite web}}: CS1 maint: multiple names: authors list (link)
  4. Glaser, Linda B. (April 21, 2022). "Chemist Song Lin honored by Chemical & Engineering News". Cornell Chronicle. Retrieved 2022-05-26.
  5. Lin, Song (2013). Elucidation of the Cation-[pi] Interaction in Small-Molecule Asymmetric Catalysis (Thesis). OCLC   870923011.
  6. Lin, Song; Jacobsen, Eric N. (October 2012). "Thiourea-catalysed ring opening of episulfonium ions with indole derivatives by means of stabilizing non-covalent interactions". Nature Chemistry. 4 (10): 817–824. Bibcode:2012NatCh...4..817L. doi:10.1038/nchem.1450. ISSN   1755-4349. PMC   3457659 . PMID   23000995.
  7. "About Song | The Lin Research Group". songlin.chem.cornell.edu. Retrieved 2022-04-09.
  8. 1 2 "Song Lin | Innovators Under 35". www.innovatorsunder35.com. Retrieved 2022-04-09.
  9. Lin, Song; Diercks, Christian S.; Zhang, Yue-Biao; Kornienko, Nikolay; Nichols, Eva M.; Zhao, Yingbo; Paris, Aubrey R.; Kim, Dohyung; Yang, Peidong; Yaghi, Omar M.; Chang, Christopher J. (2015-09-11). "Covalent organic frameworks comprising cobalt porphyrins for catalytic CO 2 reduction in water". Science. 349 (6253): 1208–1213. Bibcode:2015Sci...349.1208L. doi:10.1126/science.aac8343. ISSN   0036-8075. PMID   26292706. S2CID   4652169.
  10. Diercks, Christian S.; Lin, Song; Kornienko, Nikolay; Kapustin, Eugene A.; Nichols, Eva M.; Zhu, Chenhui; Zhao, Yingbo; Chang, Christopher J.; Yaghi, Omar M. (2018-01-24). "Reticular Electronic Tuning of Porphyrin Active Sites in Covalent Organic Frameworks for Electrocatalytic Carbon Dioxide Reduction". Journal of the American Chemical Society. 140 (3): 1116–1122. doi:10.1021/jacs.7b11940. ISSN   0002-7863. PMID   29284263. S2CID   207188096.
  11. "RSC School Seminar - Prof Song Lin (Cornell) | ANU Research School of Chemistry". chemistry.anu.edu.au. Retrieved 2022-04-09.
  12. Newton, Jennifer (May 20, 2021). "Uncovering new transformations by using electricity as a reagent". Chemistry World. Retrieved 2022-04-09.
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  14. Fu, Niankai; Sauer, Gregory S.; Saha, Ambarneil; Loo, Aaron; Lin, Song (2017-08-11). "Metal-catalyzed electrochemical diazidation of alkenes". Science. 357 (6351): 575–579. Bibcode:2017Sci...357..575F. doi: 10.1126/science.aan6206 . ISSN   0036-8075. PMID   28798126. S2CID   38654113.
  15. Zhang, Wen; Lu, Lingxiang; Zhang, Wendy; Wang, Yi; Ware, Skyler D.; Mondragon, Jose; Rein, Jonas; Strotman, Neil; Lehnherr, Dan; See, Kimberly A.; Lin, Song (April 2022). "Electrochemically driven cross-electrophile coupling of alkyl halides". Nature. 604 (7905): 292–297. Bibcode:2022Natur.604..292Z. doi:10.1038/s41586-022-04540-4. ISSN   1476-4687. PMC   9016776 . PMID   35189623.
  16. Willans, Charlotte (April 2022). "Electrification promotes tricky synthetic chemical reactions". Nature. 604 (7905): 253–254. Bibcode:2022Natur.604..253W. doi:10.1038/d41586-022-00852-7. PMID   35352045. S2CID   247791868.
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