Uncovering the Hidden Landscape of Tris(4-pyridyl) Ligands: Topological Complexity Derived from the Bridgehead

Supramolecular main group chemistry is a developing field which parallels the conventional domain of metallo-organic chemistry. Little explored building blocks in this area are main group metal-based ligands which have the appropriate donor symmetry to build desired molecular or extended arrangements. Tris(pyridyl) main group ligands (E(py)₃, E=main group metal) are potentially highly versatile building blocks since shifting the N-donor arms from the 2- to the 3-positions and 4-positions provides a very simple way of changing the ligand character from mononuclear/chelating to multidentate/metal-bridging. Here, the coordination behaviour of the first main group metal tris(4-pyridyl) ligands, E(4-py)₃ (E=Sb, Bi, Ph−Sn) is explored, as well as their ability to build metal-organic frameworks (MOFs). The complicated topology of these MOFs shows a marked influence on the counter anion and on the ability of the E(4-py)₃ ligands to switch coordination mode, depending on the steric and donor character of the bridgehead. This structure-directing influence of the bridgehead provides a potential building strategy for future molecular and MOF design in this area.     

On exponential stability analysis for neural networks with time-varying delays and general activation functions

This paper is concerned with the exponential stability analysis for a class of cellular neural networks with both interval time-varying delays and general activation functions. The boundedness assumption of the activation function is not required. The limitation on the derivative of time delay being less than one is relaxed and the lower bound of time-varying delay is not restricted to be zero. A new Lyapunov-Krasovskii functional involving more information on the state variables is established to derive a novel exponential stability criterion. The obtained condition shows potential advantages over the existing ones since no useful item is ignored throughout the estimate of upper bound of the derivative of Lyapunov functional. Finally, three numerical examples are included to illustrate the proposed design procedures and applications.     

Localization of diffusion sources in complex networks with sparse observations

Locating sources in a large network is of paramount importance to reduce the spreading of disruptive behavior. Based on the backward diffusion-based method and integer programming, we propose an efficient approach to locate sources in complex networks with limited observers. The results on model networks and empirical networks demonstrate that, for a certain fraction of observers, the accuracy of our method for source localization will improve as the increase of network size. Besides, compared with the previous method (the maximum–minimum method), the performance of our method is much better with a small fraction of observers, especially in heterogeneous networks. Furthermore, our method is more robust against noise environments and strategies of choosing observers.     

A Study of the Connectivity Over Time Behavior of On-Demand Ad Hoc Path Selection Schemes

Selecting the most appropriate path between each pair of nodes in an ad hoc network is an issue with major impact on network performance. Many schemes were proposed and compared in the literature, using various criteria. However, the connectivity over time behavior of these schemes, which is important to some practical applications, was not well studied, especially with regards to the terrain type. In this work we use simulation to study this aspect of network performance. We demonstrate that a different connectivity requirement and a different time horizon may dictate a different scheme to use. We also demonstrate that path selection schemes are not equally sensitive to the terrain.     

Optical Communications Research Activities at COM RD1 Siemens S.A.

Abstract

This article summarizes the research activities carried out by the R&D Optical Networks Communications group (COM RD1), at Siemens S.A., in collaboration with both universities and other research institutes. These activities cover various aspects of advanced modulation formats, all optical wavelength conversion, optical quality of signal monitoring in transparent WDM networks, routing, and wavelength assignment in optical networks.     

Aliphatic Polyester/polyhedral Oligomeric Silsesquioxanes Hybrid Networks via Copper‐free 1,3‐dipolar Cycloaddition Click Reaction

In this study, we describe the preparation and characterization of a new class of thermoset hybrid networks containing aliphatic polyester and polyhedral oligomeric silsesquioxanes (POSS). The copper‐free 1,3‐dipolar cycloaddition click reaction of internal alkyne functionalized aliphatic polyester and multifunctional azido POSS with different concentrations led to highly crosslinked thermoset networks. The click reactions performed under ambient conditions (i.e., in tetrahydrofuran at room temperature for 1 day) in the absence of any catalyst. The chemical composition of hybrid networks and homogenous distribution of POSS molecules were confirmed by Fourier transform infrared spectroscopy and scanning electron microscopy with energy dispersive spectroscopy. The swelling ratios of hybrid networks were commonly decreased by increasing POSS‐N₃ content and by changing polar solvents to apolar solvents. Thermogravimetric analysis results demonstrated that the thermal stability of hybrid networks increased with higher POSS feeding ratio. Tensile tests were applied to evaluate the mechanical properties of hybrid networks. Compared to neat aliphatic polyester, the mechanical properties of hybrid networks significantly improved. For instance, the tensile strength were enhanced from 5 MPa to 19 MPa by increasing the concentration of azido functionalized POSS from 10 to 40. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 2222–2227     

Morphological study of an intrinsically stretchable photovoltaic bulk heterojunction

Thin‐film polymer solar cell consisting of [6,6]‐phenyl‐C71‐butyric acid methyl ester (PC₇₁BM) and poly[[4,8‐bis[(2‐ethylhexyl)oxy]benzo[1,2‐b:4,5‐b′]dithiophene‐2,6‐diyl][3‐fluoro‐2‐[(2‐ethylhexyl)carbonyl]thieno[3,4‐b]thiophenediyl]] (PTB7) demonstrates elastic stretchability with the aid of a high boiling point additive, 1,8‐diiodooctane (DIO). The usage of DIO not only helps to form uniformly distributed nanocrystalline grains, but may also create free volumes between the nano‐grains that allow for relative sliding between the nano‐grains. The relative sliding can accommodate large external deformation. Large dichroic ratios of the optical absorption of both PC₇₁BM and PTB7 were observed under large‐strain deformation, indicating reorientation of the nanocrystalline PC₇₁BM and PTB7 polymer chains along stretching direction. The dichroic ratio decreases to nearly 1.0 as the blend was relaxed to 0% strain. Therefore, the nanometer‐size grain blending morphology provides an approach to impart stretchability to organic semiconductors that are otherwise un‐stretchable. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018 , 56, 814–820