Hong K - Search Results

1

Element-specific characterization of transient electronic structure of solvated Fe(II) complexes with time-resolved soft X-ray absorption spectroscopy.

Hong K, Cho H, Schoenlein RW, Kim TK, Huse N. Hong K, et al. Acc Chem Res. 2015 Nov 17;48(11):2957-66. doi: 10.1021/acs.accounts.5b00154. Epub 2015 Oct 21. Acc Chem Res. 2015. PMID: 26488127

2

Ligand-field symmetry effects in Fe(II) polypyridyl compounds probed by transient X-ray absorption spectroscopy.

Cho H, Strader ML, Hong K, Jamula L, Gullikson EM, Kim TK, de Groot FM, McCusker JK, Schoenlein RW, Husea N. Cho H, et al. Among authors: hong k. Faraday Discuss. 2012;157:463-74; discussion 475-500. doi: 10.1039/c2fd20040f. Faraday Discuss. 2012. PMID: 23230783

3

Femtosecond Soft X-ray Spectroscopy of Solvated Transition-Metal Complexes: Deciphering the Interplay of Electronic and Structural Dynamics.

Huse N, Cho H, Hong K, Jamula L, de Groot FM, Kim TK, McCusker JK, Schoenlein RW. Huse N, et al. Among authors: hong k. J Phys Chem Lett. 2011 Apr 21;2(8):880-4. doi: 10.1021/jz200168m. Epub 2011 Mar 30. J Phys Chem Lett. 2011. PMID: 26295622

4

Time-Resolved X-ray Spectroscopy in the Water Window: Elucidating Transient Valence Charge Distributions in an Aqueous Fe(II) Complex.

Van Kuiken BE, Cho H, Hong K, Khalil M, Schoenlein RW, Kim TK, Huse N. Van Kuiken BE, et al. Among authors: hong k. J Phys Chem Lett. 2016 Feb 4;7(3):465-70. doi: 10.1021/acs.jpclett.5b02509. Epub 2016 Jan 19. J Phys Chem Lett. 2016. PMID: 26727390

5

Tracking reaction dynamics in solution by pump-probe X-ray absorption spectroscopy and X-ray liquidography (solution scattering).

Kim J, Kim KH, Oang KY, Lee JH, Hong K, Cho H, Huse N, Schoenlein RW, Kim TK, Ihee H. Kim J, et al. Among authors: hong k. Chem Commun (Camb). 2016 Mar 7;52(19):3734-49. doi: 10.1039/c5cc08949b. Chem Commun (Camb). 2016. PMID: 26785280

6

Electronic and Molecular Structure of the Transient Radical Photocatalyst Mn(CO)5 and Its Parent Compound Mn2(CO)10.

Cho H, Hong K, Strader ML, Lee JH, Schoenlein RW, Huse N, Kim TK. Cho H, et al. Among authors: hong k. Inorg Chem. 2016 Jun 20;55(12):5895-903. doi: 10.1021/acs.inorgchem.6b00208. Epub 2016 Jun 1. Inorg Chem. 2016. PMID: 27248860

7

Light-Induced Radical Formation and Isomerization of an Aromatic Thiol in Solution Followed by Time-Resolved X-ray Absorption Spectroscopy at the Sulfur K-Edge.

Ochmann M, von Ahnen I, Cordones AA, Hussain A, Lee JH, Hong K, Adamczyk K, Vendrell O, Kim TK, Schoenlein RW, Huse N. Ochmann M, et al. Among authors: hong k. J Am Chem Soc. 2017 Apr 5;139(13):4797-4804. doi: 10.1021/jacs.6b12992. Epub 2017 Mar 27. J Am Chem Soc. 2017. PMID: 28219243

8

UV-Photochemistry of the Disulfide Bond: Evolution of Early Photoproducts from Picosecond X-ray Absorption Spectroscopy at the Sulfur K-Edge.

Ochmann M, Hussain A, von Ahnen I, Cordones AA, Hong K, Lee JH, Ma R, Adamczyk K, Kim TK, Schoenlein RW, Vendrell O, Huse N. Ochmann M, et al. Among authors: hong k. J Am Chem Soc. 2018 May 30;140(21):6554-6561. doi: 10.1021/jacs.7b13455. Epub 2018 May 17. J Am Chem Soc. 2018. PMID: 29771112

9

Transient metal-centered states mediate isomerization of a photochromic ruthenium-sulfoxide complex.

Cordones AA, Lee JH, Hong K, Cho H, Garg K, Boggio-Pasqua M, Rack JJ, Huse N, Schoenlein RW, Kim TK. Cordones AA, et al. Among authors: hong k. Nat Commun. 2018 May 18;9(1):1989. doi: 10.1038/s41467-018-04351-0. Nat Commun. 2018. PMID: 29777157 Free PMC article.

10

Following Metal-to-Ligand Charge-Transfer Dynamics with Ligand and Spin Specificity Using Femtosecond Resonant Inelastic X-ray Scattering at the Nitrogen K-Edge.

Jay RM, Eckert S, Van Kuiken BE, Ochmann M, Hantschmann M, Cordones AA, Cho H, Hong K, Ma R, Lee JH, Dakovski GL, Turner JJ, Minitti MP, Quevedo W, Pietzsch A, Beye M, Kim TK, Schoenlein RW, Wernet P, Föhlisch A, Huse N. Jay RM, et al. Among authors: hong k. J Phys Chem Lett. 2021 Jul 22;12(28):6676-6683. doi: 10.1021/acs.jpclett.1c01401. Epub 2021 Jul 14. J Phys Chem Lett. 2021. PMID: 34260255 Free PMC article.

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