Search results for "Hyperbranched polymer"
showing 3 items of 13 documents
Linear–dendritic block copolymers: The state of the art and exciting perspectives
2011
Concurrent with the rapid development of both dendrimers and hyperbranched polymers, a novel class of block copolymer architectures has emerged from the combination of these dendritic architectures with linear chains, the “linear–dendritic block copolymers” (LDBCs). This review gives a comprehensive summary of the state of the art in this rapidly developing field from pioneering early work to promising recent approaches.The different strategies leading to these hybrid architectures with either perfect dendrimer/dendron building blocks or imperfect, yet more conveniently accessible hyperbranched segments, are reviewed and compared. The consequences of the unusual polymer topology for supramo…
Hyperbranched polymer architectures: From Flory's AB(f-1) polycondensates to controlled structures
2020
Abstract Celebrating the 100th anniversary of Staudinger's “macromolecular concept”, polymer scientists critically evaluate the past developments and future challenges of polymer science, asking: Quo vadis, Macromolecular Science? The main focus in Polymer Science has been on linear polymers or crosslinked systems (elastomers and thermosets) until the late 1980ies. The advent of dendritic polymers, i.e. dendrimers and hyperbranched polymers (HBPs) attracted wide-spread attention in the polymer community. This article gives a brief overview of the developments in the area of hyperbranched polymers and demonstrates that they have since become a novel class of polymer materials.
Molecular parameters of hyperbranched polymers made by self-condensing vinyl polymerization of macroinimers
2000
The molecular weight averages and the degree of branching, DB, of a hyperbranched polymer obtained by self-condensing vinyl polymerization (SCVP) of a macroinimer A-(m)γ-B* is calculated by modifying the existing equations for SCVP. The polydispersity is lowered by a factor (γ + 1), where γ is the degree of polymerization of the macroinimer. DB decreases with γ, however, at full conversion the DB of the polymacroinimer is approximately 60% higher than expected from the “dilution” of an AB* inimer with linear m units. This is the result of the existence of a new kind of branched units. The structure of polymacroinimers is similar to the pattern of a highly branched copolymer obtained by self…