Structure–property relationships in segmented polyurethanes with metal chelates in the main chain

2000 ◽  
Vol 36 (6) ◽  
pp. 1113-1126 ◽  
Author(s):  
G. Georgoussis ◽  
A. Kanapitsas ◽  
P. Pissis ◽  
Yu.V. Savelyev ◽  
V.Ya. Veselov ◽  
...  
Polymers ◽  
2021 ◽  
Vol 13 (21) ◽  
pp. 3654
Author(s):  
Rayya A. Al-Balushi ◽  
Ashanul Haque ◽  
Idris J. Al-Busaidi ◽  
Houda Al-Sharji ◽  
Muhammad S. Khan

Metalla-ynes and poly(metalla-ynes) have emerged as unique molecular scaffolds with fascinating structural features and intriguing photo-luminescence (PL) properties. Their rigid-rod conducting backbone with tunable photo-physical properties has generated immense research interests for the design and development of application-oriented functional materials. Introducing a second d- or f-block metal fragment in the main-chain or side-chain of a metalla-yne and poly(metalla-yne) was found to further modulate the underlying features/properties. This review focuses on the photo-physical properties and opto-electronic (O-E) applications of heterometal grafted metalla-ynes and poly(metalla-ynes).


2020 ◽  
Vol 11 (39) ◽  
pp. 6251-6258
Author(s):  
Connor J. Stubbs ◽  
Andrew P. Dove

Rigid ring structures have gained increasing interest in the polymer materials community as an effective means to manipulate bulk properties. Here, we investigate structure–property relationships of the smallest ring: cyclopropane.


Molecules ◽  
2020 ◽  
Vol 25 (7) ◽  
pp. 1716 ◽  
Author(s):  
Paul Strasser ◽  
Ian Teasdale

Polymers in which phosphorus is an integral part of the main chain, including polyphosphazenes and polyphosphoesters, have been widely investigated in recent years for their potential in a number of therapeutic applications. Phosphorus, as the central feature of these polymers, endears the chemical functionalization, and in some cases (bio)degradability, to facilitate their use in such therapeutic formulations. Recent advances in the synthetic polymer chemistry have allowed for controlled synthesis methods in order to prepare the complex macromolecular structures required, alongside the control and reproducibility desired for such medical applications. While the main polymer families described herein, polyphosphazenes and polyphosphoesters and their analogues, as well as phosphorus-based dendrimers, have hitherto predominantly been investigated in isolation from one another, this review aims to highlight and bring together some of this research. In doing so, the focus is placed on the essential, and often mutual, design features and structure–property relationships that allow the preparation of such functional materials. The first part of the review details the relevant features of phosphorus-containing polymers in respect to their use in therapeutic applications, while the second part highlights some recent and innovative applications, offering insights into the most state-of-the-art research on phosphorus-based polymers in a therapeutic context.


MRS Bulletin ◽  
2010 ◽  
Vol 35 (3) ◽  
pp. 194-200 ◽  
Author(s):  
Megan L. Robertson ◽  
Marc A. Hillmyer ◽  
Anne-Cécile Mortamet ◽  
Anthony J. Ryan

AbstractHybrid macromolecules composed of two or more covalently connected segments have the ability to self-assemble into nanostructured materials. These fascinating materials are used in applications ranging from footwear to bitumen modification to microelectronics. The number of technologies that utilize or could benefit from multiphase polymers is expanding at a rapid rate. This growth is due to the development of simple scalable synthetic technologies, a deeper understanding of their structure-property relationships, and their effectiveness as low-level additives. As industrial uses of self-assembled polymers become more prevalent, there will be a heightened focus on alternative preparative approaches that do not rely on petroleum feedstocks. Therefore the development of biorenewable multiphase polymers is an important research endeavor. In this article, we will explore the synthesis, self-assembly, and properties of renewable block and graft copolymers that contain aliphatic polyesters, as well as bio-sourced segmented polyurethanes. These two classes of multiphase polymers are the most promising and practical candidates for implementation in the next generation of sustainable materials.


Author(s):  
J. Petermann ◽  
G. Broza ◽  
U. Rieck ◽  
A. Jaballah ◽  
A. Kawaguchi

Oriented overgrowth of polymer materials onto ionic crystals is well known and recently it was demonstrated that this epitaxial crystallisation can also occur in polymer/polymer systems, under certain conditions. The morphologies and the resulting physical properties of such systems will be presented, especially the influence of epitaxial interfaces on the adhesion of polymer laminates and the mechanical properties of epitaxially crystallized sandwiched layers.Materials used were polyethylene, PE, Lupolen 6021 DX (HDPE) and 1810 D (LDPE) from BASF AG; polypropylene, PP, (PPN) provided by Höchst AG and polybutene-1, PB-1, Vestolen BT from Chemische Werke Hüls. Thin oriented films were prepared according to the method of Petermann and Gohil, by winding up two different polymer films from two separately heated glass-plates simultaneously with the help of a motor driven cylinder. One double layer was used for TEM investigations, while about 1000 sandwiched layers were taken for mechanical tests.


Author(s):  
Barbara A. Wood

A controversial topic in the study of structure-property relationships of toughened polymer systems is the internal cavitation of toughener particles resulting from damage on impact or tensile deformation.Detailed observations of the influence of morphological characteristics such as particle size distribution on deformation mechanisms such as shear yield and cavitation could provide valuable guidance for selection of processing conditions, but TEM observation of damaged zones presents some experimental difficulties.Previously published TEM images of impact fractured toughened nylon show holes but contrast between matrix and toughener is lacking; other systems investigated have clearly shown cavitated impact modifier particles. In rubber toughened nylon, the physical characteristics of cavitated material differ from undamaged material to the extent that sectioning of heavily damaged regions by cryoultramicrotomy with a diamond knife results in sections of greater than optimum thickness (Figure 1). The detailed morphology is obscured despite selective staining of the rubber phase using the ruthenium trichloride route to ruthenium tetroxide.


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