Texas Tech University

Dr. Guigen Li

Li Guigen

Title: Paul W. Horn Distinguished Professor

Education: Ph.D., University of Arizona (Victor J. Hruby), 1995
Postdoctoral reseach, The Scripps Research Institute (K. Barry Sharpless, 2001 Nobel Laureate in Chemistry), 1995-97.
Played a key role in the discovery of asymmetric aminohydroxylation reaction (Sharpless AA).
Associate Editor, Molecules
Associate Editor, Frontiers in Chemistry

Research Area: Organic, Chirality, Medicinal and Bioorganic Chemistry

Office: Chemistry 300-A

Phone: 806-834-8755

Email: guigen.li@ttu.edu

Prof Li and his coworkers have achieved over 360 publications (h-index = 59). His labs are currently conducting the following research.

1. Multi-Layer 3D Chirality and Multi-Layer Polymers

(a). Li G. et al, Research, 2021, 2021: 3565791 (a Science sister journal of, by AAAS), https://spj.sciencemag.org/journals/research/aip/3565791/
(b). Li G. et al, Natl Sci Rev, 2020, https://doi.org/10.1093/nsr/nwz203;https://academic.oup.com/nsr/article/8/1/nwaa205/5899765
(c). Li G. et al, Research, 2019, 2019: 6717104 (a Science sister journal of, by AAAS), https://doi.org/10.34133/2019/6717104
(d). Li G. et al, Sci China Chem., 2020, http://engine.scichina.com/doi/10.1007/s11426-019-9711-x

Recently, Li group has discovered new multi-layer 3D chirality. The chirality is characterized by sandwich arrangement: it is composed of three almost parallel planes, with the middle plane as the central layer, one layer at the top and the other layer at the bottom of the central plane (Figures 1 & 2). The upper and lower layers are interdependent and mutually restricted to avoid the possible racemization of mirror isomers. The multi-layer 3D chiral molecules and their precursors exhibit characteristics rarely seen in normal small organic molecules: they form long bars or nest-like solids, exhibit multi-colored fluorescence and AIE, and some of them exhibit extremely strong optical rotation (Figure 2).

Previous Known Chirality

Figure 1. Well-known and new chirality types

CC Bond-Bridge Multi-Layer 3D Chirality

Figure 2. Photo properties of multi-layer 3D molecules

2. GAP Chemistry and Reagents

(Org. Biomol. Chem., 2017, 15, 1718; J. Am. Chem. Soc.,  2020, 142, 8910)

Group-Assisted-Purification (GAP) chemistry is to introduce specific functional groups into the substrates for synthetic reactions so that the products in the subsequent purification process does not need to go through column chromatography or recrystallization, only a simple washing is needed to afford pure products (Figure 3). It is the first concept combining four chemical and physical aspects together: reaction, reagents, separation, and purification. It requires efficient control of solubility, stability, reactivity and selectivity for a broad scope of reactions and synthesis.

GAP chemistry can convert organic compounds for sticky oils into solids. When GAP chemistry is utilized for peptide synthesis, it can increase chemical yields (GAsyn chemistry-group-assisted synthesis), and enables Fmoc protection group to be usable for solution-phase peptide synthesis. GAP chemistry has shown success in recovering/recycling catalysts for re-use, including organo and organometallic catalysts (in collaboration with Profs Zhang and Findlater, Figure 4).

GAP Chemistry Description

Figure 3. GAP chemistry description

Scheme: GAP Chemistry Application

Scheme 1. GAP chemistry application

Figure 4A GAP Catalyst of Recycling for ReuseFigure 4B GAP Catalyst of Recycling for Reuse

Scheme 2. GAP catalyst of recycling for re-use

3. New Catalytic Reactions and Synthetic Light-Harvesting Assembly

(J. Am. Chem. Soc., 2017, 139, 11184; Angew. Chem. Int. Ed., 2020, 59, 3078; J. Am. Chem. Soc., 2021, spotlight paper, https://dx.doi.org/10.1021/jacs.0c12853)

In collaboration with research groups of Prof Ge (Figure 5), Profs Stang and Deria (Figure 3), we conducted C-H activation/funcrionalization and synthetic light-harvesting assembly studies. (a) we achieved Pd(II)-catalyzed γ-C(sp3)–H activation of aliphatic and aromatic hetero aldehydes by using a transient ligand and an external ligand, concurrently. A wide array of γ-arylated aldehydes were readily accessed without pre-installing any internal directing groups. This reaction can be performed on gram-scale and showed its potential applications on the design and synthesis of new mechanofluorochromic materials with blue-shifted mechanochromism properties. (b) we designed and synthesized new trigonal prismatic metallacages of bearing triphenylamine and anthracene moieties to fabricate artificial light-harvesting systems (Figure 6). The new anthracene−triphenylamine chromophore makes possible the tunable excited-state property as a function of the solvent polarity, temperature, and concentration. The synergistic photophysical footprint of these metallacages, defined by their high absorptivity and emission quantum yield (QY) relative to free ligands, signifies them as a superior light sensitizer component in an LHS. In the presence of the fluorescent dye Nile Red (NR) as an energy acceptor, the metallacages display efficient (>93%) excited energy transfer to NR through an apparent static quenching mechanism in viscous dimethyl sulfoxide solvent.

Figure 5. C-H bond Activation of Aldehydes

Figure 4. C-H bond activation of aldehydes

Figure 5. Synthetic Light-Harvesting Assembly for Energy Transfer

Figure 5. Synthetic light-harvesting assembly for energy transfer

Department of Chemistry & Biochemistry