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Development of biobased aliphatic polyesters with better mechanical (tensile) properties in film has attracted considerable attention. This report presents the synthesis of soluble network biobased aliphatic polyesters by acyclic diene metathesis (ADMET) polymerization of bis(undec-10-enyl)isosorbide diester [M1, dianhydro-D-glucityl bis(undec-10-enoate)] in the presence of a tri-arm crosslinker [CL, glycerol tris(undec-10-enoate)] using a ruthenium–carbene catalyst, and subsequent olefin hydrogenation using RhCl(PPh3)3. The resultant polymers, after hydrogenation (expressed as HCP1) and prepared in the presence of 1.0 mol% CL, showed better tensile properties than the linear polymer (HP1) with similar molecular weight [tensile strength (elongation at break): 20.8 MPa (282%) in HP1 vs. 35.4 MPa (572%) in HCP1]. It turned out that the polymer films prepared by the addition of CL during the polymerization (expressed as a 2-step approach) showed better tensile properties. The resultant polymer film also shows better tensile properties than the conventional polyolefins such as linear high density polyethylene, polypropylene, and low density polyethylene. [ABSTRACT FROM AUTHOR]

A lot of oil is leaked into aquatic environments, significantly impacting fish health and, consequently, human populations. This study aimed to introduce an L-phenylalanine-based low-molecular-weight gelator (expressed as Z-Phe-C18) as a smart remediation tool for oil spills. Several groups of Nile tilapia were allocated in aquaria exposed to different doses of crude engine oil with/without the organogelator for 4 weeks. The results revealed a significant increase in biochemical oxygen demand, chemical oxygen demand, electrical conductivity, and total dissolved solids in water samples of fish aquaria exposed to oil pollution. The antioxidant activity levels, micronucleus formation, and expression patterns of stress-related genes were significantly higher in the livers of fish exposed to crude oil than in those of control fish. On the contrary, fish groups exposed to oil pollution and treated with the organogelator indicated that antioxidant enzymes, micronucleus incidence, and gene expression alteration of stress-related genes declined compared with those exposed to oil pollution only. The results suggest that oil pollution can induce oxidative stress via the enhancement of oxygen free radical formation. On the contrary, oil removal by the organogelator decreases oxidative stress and consequently strengthens fish immunity. So, we can conclude that organogelator treatment is promoting oxidative resistance development by increasing the activities of antioxidant enzymes, which are important in protection against oil pollution and preventing peroxidation of fish tissues. Promisingly, the organogelator could be used as a tool for the remediation of oil pollution in aquatic environments. [ABSTRACT FROM AUTHOR]

Defect-free, highly trans oligo(2,5-dialkoxy-1,4-phenylene vinylene)s [alkoxy = O(CH2)2OSi iPr3] with both repeat units (ex. 9, 15, and 31 repeat units) and end groups (aldehyde, C6F5, terthiophene, ferrocene) well-defined are prepared by a stepwise combined olefin metathesis using Mo(CHCMe2Ph)(N-2,6-Me2C6H3)[OCCH3(CF3)2]2 with subsequent Wittig-type coupling. End-functionalized oligomers with uniform distributions are also prepared by acyclic diene metathesis (ADMET) condensation using a ruthenium-carbene catalyst, followed by the above combined olefin metathesis and Wittig coupling. The effects of the repeat units and the end functional groups on the optical properties are explored; the photoluminescence quantum yields in the end-functionalized oligomers (e.g., 9 mers) are affected by the end groups. [ABSTRACT FROM AUTHOR]

The precise synthesis of chemically, analytically pure oligo(2,5-dialkoxy-1,4-phenylene vinylene)s [OPVs, alkoxy = O(CH2)2OSiiPr3] with strictly controlled repeat units (up to 15 repeat units) and well-defined end groups has been achieved by a combined olefin metathesis reaction of 2,5-dialkoxy-1,4-divinylbenzene or their derivatives with a molybdenum–alkylidene complex and the subsequent Wittig-type cleavage with their dicarboxaldehyde analogues. The effects of the repeat units and the end functional groups toward their UV–vis and the fluorescence spectra have been clearly demonstrated. [ABSTRACT FROM AUTHOR]

Acyclic diene metathesis (ADMET) copolymerization of dianhydro-D-glucityl bis(undec-10-enoate) (M1) with 1,9-decadiene (DCD) using ruthenium-carbene catalyst, RuCl2(IMesH2)(CH-2-OiPr-C6H4) [IMesH2 = 1,3-bis(2,4,6-trimethylphenyl)imidazolin-2-ylidene, HG2], afforded unsaturated polyesters (Mn = 9300–23,400) under the optimized conditions. Subsequent tandem hydrogenation (H2 1.0 MPa, 50 °C) with the addition of a small amount of Al2O3 resulted in the saturated polymers having a melting temperature of 71.7–107.6 °C, depending on the molar ratio of M1 and DCD. [ABSTRACT FROM AUTHOR]

Acyclic diene metathesis (ADMET) polymerization of biobased α,ω-dienes of bis(undec-10-enoate) with diols (1,4-butanediol, isosorbide, isomannide, and 1,4-cyclohexanedimethanol) afforded high-molecular weight unsaturated polyesters, and subsequent tandem hydrogenation (H 2 1.0 MPa, 50 °C, 3 h) gave the saturated polymers upon addition of a small amount of Al 2 O 3 (1.0-1.7 wt %). Subsequent reaction of the unsaturated polymers with ethylene afforded the oligomers (by depolymerization and degradation)., Competing Interests: The authors declare no competing financial interest., (Copyright © 2020 American Chemical Society.)

Various block (graft) copolymers have been prepared by combination of acyclic diene metathesis (ADMET) polymerization of 9,9-dialkyl-2,7-divinyl-fluorene with Cu-catalyzed atom transfer radical polymerization (ATRP) of styrene using macroinitiators prepared by introduction of initiating functionalities into poly(9,9-dialkylfluorene-2,7-vinylene)s (PFVs) chain ends: a precise synthesis of the amphiphilic ABCBA-type block copolymers has also been attained by subsequent combination with click reaction after modification of the chain end with NaN 3 .