Fully Room-Temperature Reprogrammable, Reprocessable, and Photomobile Soft Actuators from a High-Molecular-Weight Main-Chain Azobenzene Crystalline Poly(ester-amide)

Author(s):  
Yan Zhou ◽  
Lei Wang ◽  
Shengkui Ma ◽  
Huiqi Zhang
2019 ◽  
Vol 10 (23) ◽  
pp. 3097-3106 ◽  
Author(s):  
Robin M. Cywar ◽  
Jian-Bo Zhu ◽  
Eugene Y.-X. Chen

A ring-fused γ-butyrolactone can be selectively ring-open polymerized at room temperature by N-heterocyclic carbenes to cyclic polyester or by bifunctional (thio)urea and base pairs in a living fashion to high molecular weight linear polyester that can be organocatalytically and quantitatively recycled at 120 °C.


2017 ◽  
Vol 46 (21) ◽  
pp. 6843-6847 ◽  
Author(s):  
F. Anke ◽  
D. Han ◽  
M. Klahn ◽  
A. Spannenberg ◽  
T. Beweries

The complex [(PNHP)Fe(H)(CO)(HBH3)] (PNHP = HN(CH2CH2Pi-Pr2)2) serves as a catalyst precursor for the selective dehydrocoupling of methylamine borane at room temperature, tentatively via an off-metal polymerisation pathway.


1973 ◽  
Vol 19 (12) ◽  
pp. 1339-1344 ◽  
Author(s):  
Stuart J Updike ◽  
John D Simmons ◽  
Douglas H Grant ◽  
Judith A Magnuson ◽  
Theodore L Goodfriend

Abstract A technique of radioimmunoassay is presented that eliminates pipetting and centrifugation, and excludes interferences by high-molecular-weight materials from the incubation and separation steps. A solid-phase binding reagent is prepared by first entrapping antibody in polyacrylamide gel. This gel is then fragmented, sieved, dried with ethanol or lyophilized, and placed in miniature disposable chromatographic columns. Application of the sample to the intra-gel column compartment is determined by the water regain of the gel. This pipetless method of sample application depends on reproducible aliquots of dry gel particles in every column. A method for preloading radiolabeled hormone and standard hormone into the column is also described. This technique has been successfully applied to the assay of angiotensin I and insulin. Dry antibody—gel stored at room temperature for 26 months has not shown loss of binding activity.


2018 ◽  
Author(s):  
Bryan Joshua Jones ◽  
Advitiya Mahajan ◽  
Alptekin Aksan

Dextranol, a reduced dextran, prevents damage to stored dry protein samples that unmodified dextran would otherwise cause. Lyoprotectants like the polysaccharide dextran are critical for preserving dried protein samples by forming rigid a glass that protects entrapped protein molecules. Stably dried proteins are important for maintaining critical information in clinical samples like blood serum. However, we found that dextran reacts with serum proteins during storage, producing high-molecular weight Amadori-product conjugates. These conjugates appeared in a matter of days or weeks when stored at elevated temperatures (37° or 45°C), but also appeared on a timescale of months when stored at room temperature. We synthesized a less reactive dextranol by reducing dextran’s anomeric carbon from an aldehyde to an alcohol. Serum samples dried in a dextranol-based matrix protected the serum proteins from forming high-molecular weight conjugates. The levels of four cancer-related serum biomarkers (prostate specific antigen, neuropiln-1, osteopontin, and metalloproteinase 7) decreased, as measured by immunoassay, when serum samples were stored for one to two weeks in dextran-based matrix. Switching to a dextran-based lyoprotection matrix slightly reduced the damage to osteopontin and completely stopped any detectable damage during storage in the other three biomarkers when for a period of two weeks at 45°C. Dextranol offers a small and easy modification to dextran that significantly improves the molecule’s function as a lyoprotectant by eliminating the potential for damaging protein-polysacharide conjugation.


2021 ◽  
Author(s):  
Hongfeng Zhang ◽  
Paul Bicho ◽  
Erin A.S. Doherty ◽  
Richard J. Riehle ◽  
Jose Moran Mirabal ◽  
...  

Abstract Poly(ethylene-alt-maleic acid), PEMAc, is a linear polymer that, along with its isomer polyacrylic acid, has the highest carboxylic acid content of any polymer. The goal of this work was to elucidate the mechanisms that control the amount of PEMAc that is permanently fixed on pulp fibers after the impregnation of dry pulp with a dilute PEMAc solution followed by drying/heating (curing). Two mechanisms by which PEMAc is fixed to cellulose fibers were discovered, chemical, and physical fixation. With room temperature drying only physical fixation is operative. Evidence supports the explanation that physical fixation is a consequence of the slow swelling and dissolution of thick dried PEMAc deposits on fiber surfaces. Chemical fixation includes grafting to cellulose plus enhanced cohesion within thick PEMAc layers, possibly due to interchain crosslinking. The pH of the PEMAc impregnation solution determines the fixation mechanism for curing temperatures above 100 o C. Physical fixation dominates when pH > 8 whereas chemical fixation dominates for impregnation pH values < 7, suggesting the curing reactions require partial or complete protonation of the succinic acid moieties. The yield of impregnated polymer fixed to the fibers after washing depends upon the fixation mechanism. When chemical fixation dominates, the yields for low and high molecular weight PEMAc doses less than 0.1 meq/g (6.3 kg PEMA/tonne dry pulp) were close to or equaled 100%. By contrast, when the primary mechanism is physical fixation, yields are ~50% for high molecular weight PEMAc and 0-20% for low MW PEMAc. These results show that high PEMAc fixation yields can be achieved under curing conditions that could be implemented in pulp drying machines producing dry market pulp.


2017 ◽  
Vol 53 (85) ◽  
pp. 11701-11704 ◽  
Author(s):  
Diego A. Resendiz-Lara ◽  
Naomi E. Stubbs ◽  
Marius I. Arz ◽  
Natalie E. Pridmore ◽  
Hazel A. Sparkes ◽  
...  

High molecular weight B-arylated polyaminoboranes are obtained via catalytic dehydropolymerisation of B-aryl amine–boranes and represent the first inorganic polystyrene analogues with a B–N main chain.


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