Self-assembly of noble metal nanoparticles into sub-100 nm colloidosomes with collective optical and catalytic properties.

Self-assembly at the nanoscale represents a powerful tool for creating materials with new structures and intriguing collective properties. Here, we report a novel strategy to synthesize nanoscale colloidosomes of noble metals by assembling primary metal nanoparticles at the interface of emulsion droplets formed by their capping agent. This strategy produces noble metal colloidosomes of unprecedentedly small sizes (<100 nm) in high yield and uniformity, which is highly desirable for practical applications. In addition, it enables the high tunability of the composition, producing a diversity of monometallic and bimetallic alloy colloidosomes. The colloidosomes exhibit interesting collective properties that are different from those of individual colloidal nanoparticles. Specifically, we demonstrate Au colloidosomes with well-controlled interparticle plasmon coupling and Au-Pd alloy colloidosomes with superior electrocatalytic performance, both thanks to the special structural features that arise from the assembly. We believe this strategy provides a general platform for producing a rich class of miniature colloidosomes that may have fascinating collective properties for a broad range of applications

A study of the interaction between inverted cucurbit[7]uril and symmetric viologens

The interaction between inverted cucuribit[7]uril (iQ[7]) and a series of symmetric viologen derivatives bearing aliphatic substituents of variable length, namely dicationic dialkyl-4,4′-bipyridinium guests where the alkyl is CH₃(CH₂)n with n = 0 to 6, has been studied in aqueous solution by ¹H NMR spectroscopy, electronic absorption spectroscopy, isothermal titration calorimetry and mass spectrometry. In the case of both n = 5 (HV ²⁺) and 6 (SV²⁺), single crystal X-ray diffraction revealed the composition to be [(iQ[7])₂(HV)₂][CdCl₃Br][H₃O+]₂[H₂O]₁₂.₅ and (iQ[7])₂(C7-SV)₁.₅[CdCl₄]₄(H₃O⁺)₅(H₂O)₈, respectively, with both adopting an external B-type structure (the alkyl chains of the viologen reside within the iQ[7])

Supramolecular assembly of cucurbit[6]uril and N-butyl-4-pyrrolidinopyridine

The nature of the supramolecular host-guest complex involving 4-pyrrolidinopyridine (BuPC4) and cucurbit[6]uril (Q[6]) has been investigated by NMR and UV spectroscopy, MALDI-TOF mass spectrometry, X-ray crystallography and isothermal titration calorimetry (ITC). The results revealed that the alkyl chain of the guest BuPC4 is located inside the cavity of the Q[6] host, whereas the other section of the BuPC4 guest remains outside of the portal

Measurement to radius of Newton’s ring fringes using polar coordinate transform

Background: Newton’s ring method is often used to measure many physical parameters. And some measured physical quantity can be extracted by calculating the radius parameter of circular fringes from Newton's ring configuration. Methods: The paper presents a new measuring method for radius of circular fringes, which includes three main steps, i.e., determination of center coordinates of circular fringes, polar coordinates transformation of circular fringes, and gray projection of the transformed result which along the horizontal direction. Then the radius values of each order ring are calculated. Results: The simulated results indicate that the measuring accuracy of the radius under the effect of random noise can keep the degree of less than 0.5 pixels. Conclusions: The proposed method can obtain the radius data of each order closed circular fringes. Also, it has several other advantages, including ability of good anti-noise, sub-pixel accuracy and high reliability, and easy to in-situ use