Zifei Lu

ORCID: 0000-0002-6710-2808
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Research Areas
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Molecular Junctions and Nanostructures
  • Supramolecular Self-Assembly in Materials
  • Supramolecular Chemistry and Complexes
  • Luminescence and Fluorescent Materials
  • Fullerene Chemistry and Applications
  • Graphene research and applications
  • Organic Electronics and Photovoltaics
  • Synthesis and Properties of Aromatic Compounds
  • Metal-Organic Frameworks: Synthesis and Applications
  • Advanced Chemical Physics Studies
  • Magnetism in coordination complexes
  • Advanced biosensing and bioanalysis techniques
  • Advanced Biosensing Techniques and Applications
  • Porphyrin and Phthalocyanine Chemistry
  • Molecular Sensors and Ion Detection
  • Biosensors and Analytical Detection
  • Lanthanide and Transition Metal Complexes

University of Cambridge
2021-2023

Royal Society of Chemistry
2023

Cambridge Consultants (United Kingdom)
2023

Xiamen University
2018

Collaborative Innovation Center of Chemistry for Energy Materials
2018

An enantiopure ligand with four bidentate metal-binding sites and (S)-carbon stereocenters self-assembles octahedral ZnII or CoII to produce O-symmetric M8L6 coordination cages. The Λ- Δ-handedness of the metal centers forming corners these cages is determined by solvent environment: same (S)-ligand produces one diastereomer, (S)24-Λ8-M8L6, in acetonitrile but another opposite metal-center handedness, (S)24-Δ8-M8L6, nitromethane. Van 't Hoff analysis revealed Δ stereochemical configuration...

10.1021/jacs.2c00245 article EN cc-by Journal of the American Chemical Society 2022-04-02

Here we demonstrate how the hydrogen-bonding ability of a BINOL-based dialdehyde subcomponent dictated stereochemical outcome its subsequent self-assembly into one diastereomeric helicate form when bearing free hydroxy groups, and another in case methylated congener. The presence methyl groups also altered self-sorting behavior mixed with another, short linear subcomponent, switching system from narcissistic to integrative self-sorting. In all cases, axial chirality BINOL building block...

10.1021/jacs.1c05172 article EN cc-by Journal of the American Chemical Society 2021-06-14

We report the construction of three structurally distinct self-assembled architectures: FeII12L12 pseudoicosahedron 1, FeII2L3 helicate 2, and FeII4L4 tetrahedron 3, formed from a single triazatriangulenium subcomponent A under different reaction conditions. Pseudoicosahedral capsule 1 is largest through self-assembly to date, with an outer-sphere diameter 5.4 nm cavity volume 15 nm3. The outcome depended upon concentration, where formation was favored at higher concentrations, while 2...

10.1021/jacs.1c11536 article EN Journal of the American Chemical Society 2022-01-11

Paper-based assays such as lateral flow are good candidates for portable diagnostics owing to their user-friendly format and low cost.

10.1039/c8lc00010g article EN Lab on a Chip 2018-01-01

Abstract Biomolecular systems show how host–guest binding can induce changes in molecular behavior, which turn impact the functions of system. Here we report an artificial system where dynamic adaptation during guest alters both host conformation and dynamics. The self-assembled cage employed here possesses concave walls a chirotopic cavity. Complementarity between curved surfaces fullerenes inner surface cavity leads to reconfigure stereochemically order bind these guests optimally....

10.1038/s41467-021-24344-w article EN cc-by Nature Communications 2021-07-02

Abstract Organic semiconductors are promising for efficient, printable optoelectronics. However, strong excited‐state quenching due to uncontrolled aggregation limits their use in devices. We report on the self‐assembly of a supramolecular pseudo‐cube formed from six perylene diimides (PDIs). The rigid, shape‐persistent cage sets distance and orientation PDIs suppresses intramolecular rotations vibrations, leading non‐aggregated, monomer‐like properties solution solid state, contrast fast...

10.1002/anie.202216729 article EN cc-by Angewandte Chemie International Edition 2023-01-18

Abstract Organic semiconductors are promising for efficient, printable optoelectronics. However, strong excited‐state quenching due to uncontrolled aggregation limits their use in devices. We report on the self‐assembly of a supramolecular pseudo‐cube formed from six perylene diimides (PDIs). The rigid, shape‐persistent cage sets distance and orientation PDIs suppresses intramolecular rotations vibrations, leading non‐aggregated, monomer‐like properties solution solid state, contrast fast...

10.1002/ange.202216729 article EN cc-by Angewandte Chemie 2023-01-18

Metal-organic cages have served as masks to effect the regioselective functionalization of C60. The enantioselective C60 remains challenging, however, requiring complex chiral tethers or challenging chromatography. We report a means defining up six stereocentres on C60, achieving both and fullerene functionalisation. This method involves stereochemical information transfer from formylpyridine, through framework an enantiopure cage incorporating it, series regio- stereochemically defined...

10.26434/chemrxiv-2022-l5zk8-v2 preprint EN cc-by-nc-nd 2022-07-05

10.1016/j.chempr.2022.10.014 article EN publisher-specific-oa Chem 2022-11-01

A supramolecular chromophore cube based on perylene diimides (PDIs) is reported by Sascha Feldmann and co-workers in their Research Article (e202216729). The rigid shape-persistent cage preserves the electronic purity of its PDI constituents enables observation delayed fluorescence because bright excited multimer state, acting as an excitation reservoir. Self-assembly can thus serve a powerful tool for controlling properties molecular electronics devices. Batteries Bioinorganic Chemistry...

10.1002/ange.202301806 article EN Angewandte Chemie 2023-02-15

Permissions Request permissions Contents list RSC Appl. Polym., 2023, 1, 127 DOI: 10.1039/D3LP90009F This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this in other publications without requesting further the RSC, provided that correct acknowledgement given. Read more about how to correctly acknowledge content.

10.1039/d3lp90009f article EN cc-by RSC Applied Polymers 2023-01-01

Metal-organic cages have served as masks to effect the regioselective functionalization of C60. The enantioselective C60 remains challenging, however, requiring complex chiral tethers or challenging chromatography. We report a means defining up six stereocentres on C60, achieving both and fullerene functionalisation. This method involves stereochemical information transfer from formylpyridine, through framework an enantiopure cage incorporating it, series regio- stereochemically defined...

10.26434/chemrxiv-2022-l5zk8 preprint EN cc-by-nc-nd 2022-02-03

Small molecule organic semiconductors hold great promise for efficient, printable, and flexible optoelectronic applications like solar cells displays. However, strong excited-state quenching due to uncontrolled aggregation currently limits their performance employability in devices. Here, we report on the self-assembly of a supramolecular pseudo-cube formed from six modified tetradentate perylene diimides (PDIs). The rigid, shape-persistent cage sets distance orientation PDI chromophores...

10.48550/arxiv.2210.16420 preprint EN other-oa arXiv (Cornell University) 2022-01-01
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