Publications by authors named "Dahai Zhou"

The Fano resonance in single-molecule junctions could be created by interaction with discrete and continuous molecular orbitals and enables effective electron transport modulation between constructive and destructive interference within a small energy range. However, direct observation of Fano resonance remains unexplored because of the disappearance of discrete orbitals by molecule-electrode coupling. We demonstrated the room-temperature observation of Fano resonance from electrochemical gated single-molecule conductance and current-voltage measurements of a para-carbazole anion junction.

View Article and Find Full Text PDF

The gating of charge transport through single-molecule junctions is considered a critical step towards molecular circuits but remains challenging. In this work, we report an electrostatic gating method to tune the conductance of single-molecule junctions using the scanning tunneling microscope break junction (STM-BJ) technique incorporated with a back-gated chip as a substrate. We demonstrated that the conductance varied at different applied gating voltages (Vgs).

View Article and Find Full Text PDF

Molecular potentiometers that can indicate displacement-conductance relationship, and predict and control molecular conductance are of significant importance but rarely developed. Herein, single-molecule potentiometers are designed based on ortho-pentaphenylene. The ortho-pentaphenylene derivatives with anchoring groups adopt multiple folded conformers and undergo conformational interconversion in solutions.

View Article and Find Full Text PDF

Molecular assembly is crucial in functional molecular materials and devices. Among the molecular interactions that can form assemblies, stacking among π-conjugated molecular backbones plays an essential role in charge transport through organic materials and devices. The single-molecule junction technique allows for the application of an electric field of approximately 10 V/m to the nanoscale junctions and to investigate the electric field-induced assembly at the single-stacking level.

View Article and Find Full Text PDF

A sterically demanding silaamidine (ArN = Si(L)NHAr) ligand was synthesized and employed for the preparation of a yttrium dialkyl complex, which catalytically enabled the cyclotrimerization of isocyanate with high activity and excellent functional group tolerance.

View Article and Find Full Text PDF

A series of novel chiral nonmetallocene pincer-type rare-earth metal dialkyl complexes bearing the chiral monoanionic tridentate ₂-symmetric 1,3-bis(oxazolinymethylidene)isoindoline (BOXMI-H) ligand (BOXMI)Ln(CH₂SiMe₃)₂ 1⁻3 (1: Ln = Sc, yield = 57%; 2: Ln = Lu, yield = 55%; 3: Ln = Y, yield = 62%) have been prepared in moderate yields via the acid-base reaction between the BOXMI ligand and rare-earth metal tri(trimethylsilylmethyl) complexes. The X-ray diffractions show that both of the complexes 1 and 2 contain one BOXMI ligand and two trimethylsilylmethyl ligands, adopting a distorted trigonal bipyramidal configuration. In the presence of a cocatalyst such as borate and AlR₃, these complexes 1⁻3 exhibit high activities of up to 6.

View Article and Find Full Text PDF

Renal cell carcinoma (RCC), one of the most common kidney cancers, has a poor prognosis. Epithelial to mesenchymal transition (EMT) is a hallmark of carcinoma invasion and metastasis. Several studies have examined the molecular regulation of EMT, but the relationship between histone demethylases and EMT is little understood.

View Article and Find Full Text PDF
Article Synopsis
  • The study investigates the genetic mutations of the VHL tumor-suppressor gene in a Chinese family with non-syndromic pheochromocytomas (PCCs) and individuals with sporadic PCCs (ASP).
  • DNA samples were analyzed from 20 family members and 41 ASP patients, revealing three novel mutations in the VHL gene, all associated with specific types of VHL syndrome.
  • The findings suggest that these mutations impair pVHL function, aiding in early diagnosis and treatment of Von Hippel-Lindau syndrome and advancing research on its underlying causes.
View Article and Find Full Text PDF
Article Synopsis
  • - The study aimed to analyze the VHL gene in 41 Chinese patients with sporadic pheochromocytoma by extracting DNA from blood and tumor samples, comparing it to DNA from 50 healthy individuals.
  • - Genetic testing revealed significant mutations in the VHL gene, including a mutation at nucleotide 572 and frameshift mutations from two small insertions, with some family members also carrying these mutations.
  • - The findings suggest that genetic testing for VHL mutations should be routine for patients under 50 with sporadic pheochromocytoma, as it could help diagnose hereditary forms of the condition.
View Article and Find Full Text PDF

Objective: To detect the VHL gene mutations in a Chinese family with nonsyndromic pheochromocytoma.

Methods: Mutations of VHL gene were detected in a Chinese family with nonsyndromic pheochromocytoma. Five patients and fifteen relatives were involved in this study.

View Article and Find Full Text PDF