On November 3, 2021, the 2020 National Science and Technology Award conference was held in the Great Hall of the people. "Chelation chemistry of carbon chain and metal", the scientific research achievement of Haiping Xia 's team won the second prize of the National Natural Science Award. Haiping Xia and Hong Zhang attended the award ceremony in Beijing.
Prof. Haiping Xia received the prestigious Huang Yao-zeng Organometallic Chemistry Award of the Chinese Chemical Society in 2016 in the 19th National Conference on Organometallic Chemistry on China.
Author profile of Prof. Xia was published in Angew. Chem. Int. Ed., for our group has recently published the 10th article in Angew. Chem. Int. Ed. in the last 10 years since 2004.
Aromaticity, one of the most fundamental concepts in organic chemistry, provides intrinsic stabilisation for cyclic compounds as a result of the delocalisation of π electrons. Currently, aromatic compounds (e.g., benzene, benzene derivatives, porphyrins, fullerenes, carbon nanotubes and graphene) have been applied in almost every field, including chemical engineering, biomedicine, materials science, energy science and environmental science.
We reported the first case of high-tensile and anti-aromatic carbon dragon compound, the metal bridgehead indene. The results were published online in the Journal of the American Chemical Society under the title "Isolation, Reactivity, and Tunable Properties of a Strained Antiaromatic Osmacycle." Am. Chem. Soc.
We report the preparation method of the first Craig anti-aromatic species, and analyze the nature and driving force of antiaromatic species combined with theoretical calculation system. Thus, two centuries after the discovery of the first aromatic species (naphthalene), the puzzle of the π aromatic system was perfected . The results were published online in the Proceedings of the National Academy of Sciences under the title "Synthesis and Characterization of Craig-type Antiaromatic Species with [4n + 2] π Electrons"
We have made another important advance in the field of "carbon dragon chemistry": we proposed a strategy based on π- and σ-aromatic relay drive, realizing the first metal heterocyclic butadiene to metal heterocyclic propylene ring shrinkage reaction. The results were published online in Nature Synthesis under the title "Ring Contraction of Metallacyclobutadiene to Metallacyclopropene Driven by π- and σ-Aromaticity Relay"
We synthesized a "carbon dragon complex" with an absorption spectrum of NIR-II (Near Infrared Region II). The results were published online in Angew under the title "Condensed Osmaquinolines with NIR-II Absorption Synthesized by Aryl C-H Annulation and Aromatization". Chem., Int. Ed
We describe a heterometallic [Os-Cu] complex with the characteristics of bimetallics, metallaaromatics, and pincer complexes. This complex serves as a highly effective catalyst for selective amino- and oxyselenation of unactivated alkenes. More than 80 examples including challenging substrates of unsymmetric aliphatic alkenes and amine-based nucleophiles in such reactions are provided.
We directly employed metalla-aromatics to develop EAS reactions of Craig-Möbius aromatics with excellent efficiency and remarkable regioselectivity, and the reactions were quantified in computational studies to further rationalize the preferred sites of attack on the different aromatic rings.
we use a series of synthesized (carbolong-derived) organometallic complexes as CILs to tune the electrode WF in inverted PSCs. Photovoltaic devices based on a Ag cathode, which was modified with these organometallic complexes, received a boosted PCE up to 21.29% and a remarkable fill factor that reached 83.52%, which are attributed to the dipole-enhanced carrier transport.
Congratulations to Chen, S.; Gao, X.; Hua, Y.; Peng, L. and Zhang, Y.! Their Article "Addition of Alkynes and Osmium Carbynes towards Functionalized dπ–pπ Conjugated Systems. " was accepted by [Nat. Comm.].
Polydentate complexes containing combinations of nitrogen and carbon (N and C) ligating atoms are among the most fundamental and ubiquitous molecules in coordination chemistry, yet the formation of such complexes with planar high-coordinate N/C sites remains challenging. Herein, we demonstrate an efficient route to access related complexes with tetradentate CCCN and pentadentate CCCCN and NCCCN cores by successive modification of the coordinating atoms in complexes with a CCCC core.
The discovery of new aromatic molecular frameworks has been one of the most attracting works for synthetic chemists. However, the design and synthesis of aromatic molecules with more than three fused-rings sharing a bridgehead atom is challenging and has never been achieved.
Congratulations! Our work “Successive modification of polydentate complexes gives access to planar carbon- and nitrogen-based ligands” (Nat. Commun. 2019, 10, 1488) was selected as Nature Communications Editors' Highlights. .