02687nas a2200361 4500008004100000022001400041245021300055210006900268260000800337300001400345490000700359520141200366653002201778653002601800653003401826653001101860653001301871653001501884653001401899653002301913653002401936653002501960653003301985653002502018653001802043653002502061653001302086100002302099700002002122700002302142700002802165856013202193 2017 eng d a0887-624X00aPartially bio-based poly(amide imide)s by polycondensation of aromatic diacylhydrazides based on lignin-derived phenolic acids and aromatic dianhydrides: synthesis, characterization, and computational studies0 aPartially biobased polyamide imides by polycondensation of aroma cNOV a3636-36450 v553 a

Two new bio-based diacylhydrazide monomers, namely, 4,4-(propane-1,3-diylbis(oxy))bis(3-methoxybenzohydrazide) and 4,4-(propane-1,3-diylbis(oxy))bis(3,5-dimethoxybenzohydrazide) were synthesized starting from lignin-derived phenolic acids, namely, vanillic acid and syringic acid. A series of poly(amide imide)s was synthesized by polycondensation of these diacylhydrazide monomers with commercially available aromatic dianhydrides. Poly(amide imide)s showed inherent viscosity in the range 0.44-0.56 dLg(-1) and exhibited good solubility in organic solvents. Poly(amide imide)s could be cast into transparent, flexible, and tough films from their N,N-dimethylacetamide solutions. Poly(amide imide)s showed 10% weight loss in the temperature range 340-364 degrees C indicating their good thermal stability. Glass transition temperature (T-g) of poly(amide imides)s were measured by DSC and DMA which were in the range 201-223 degrees C and 214-248 degrees C, respectively. The T-g values of poly(amide imide)s were dependent on the number methoxy substituents on aromatic rings of diacylhydrazide monomers. Molecular dynamics simulation studies revealed that chain rigidity is the dominant factor for observed trends in T-g. (c) 2017 Wiley Periodicals, Inc.

10aBiobased Polymers10aComputational studies10aGlass-transaction temperature10alignin10aMonomers10aPlant oils10aPolyimide10aReneable resources10aRenewable resources10aStep-growth polymers10astructure-property relations10aSustanaible Polymers10aThermal night10aThermosetting resins10aVanillin1 aKuhire, Sachin, S.1 aSharma, Pragati1 aChakrabarty, Suman1 aWadgaonkar, Prakash, P. uhttps://library.ncl.res.in/content/partially-bio-based-polyamide-imides-polycondensation-aromatic-diacylhydrazides-based-lignin01041nas a2200229 4500008004100000022001400041245005200055210004600107260000800153300001200161490000700173520039500180653002700575653001700602653001600619653002100635653002000656653001300676100002500689700001900714856007800733 2018 eng d a0039-788100aFirst total synthesis of (+/-)-rhodoconferimide0 aFirst total synthesis of rhodoconferimide cFEB a658-6620 v503 a

Starting from vanillin and dimethyl maleate, a concise and efficient racemic total synthesis of the potent antioxidant marine natural product (+/-)-rhodoconferimide has been carried out via the Wittig reaction, catalytic hydrogenation, selective brominations, and imide formation. An appropriate regioselective double bromination of the aromatic ring was a key step in the synthesis.

10a(+/-)-rhodoconferimide10aAntioxidants10aBromination10aNatural products10aTotal synthesis10aVanillin1 aPandhade, Kailas, R.1 aArgade, N., P. uhttps://library.ncl.res.in/content/first-total-synthesis-rhodoconferimide02050nas a2200229 4500008004100000022001400041245008400055210006900139260000800208300001100216490000800227520128700235653001301522653003201535653001301567653002701580653001301607100002701620700003701647700002701684856010901711 2023 eng d a0021-899500aEvaluation of the adhesive properties of vanillin-derived polyhydroxy urethanes0 aEvaluation of the adhesive properties of vanillinderived polyhyd cDec ae546470 v1403 a

Poly(hydroxy urethanes) (PHUs) have been considered attractive and safer variants of conventional polyurethanes (PUs). To improve the prerequisites of green and sustainable chemistry herein, we propose the synthesis and utilization of cyclic carbonate monomers majorly derived from vanillin, a lignin derivative, and CO2 for the development of PHUs. Kinetic evaluation on the polymerization temperature ascertained 80 degrees C as the optimum condition for PHU synthesis. The structural evaluation of PHUs was carried out by various spectroscopic techniques, such as FTIR, (HNMR)-H-1, and C-13-NMR, molar masses were determined by gel permeation chromatography (Mn varied between 2500 and 11,100 g/mol), and thermal properties evaluated by differential scanning calorimeter (Tg in the ranges of 28-42 degrees C), and thermogravimetric analysis (stable above 180 degrees C). Since the PHUs are enriched with pendant hydroxyl groups on their backbone which can promote adhesion, lap shear studies on the aluminum substrate exhibited a maximum shear strength of 1.65 +/- 0.37 MPa. This study demonstrates an attractive and environment-friendly pathway for developing novel PHUs network using renewable biobased resources and further explores its applicability as adhesives.

10aadhesive10abiobased cyclic dicarbonate10adiamines10apoly(hydroxyurethane)s10aVanillin1 aGhuge, Gorakh, Hiraman1 aKambikanam, Karthika, Vayalacher1 aNair, Kiran, Sukumaran uhttps://library.ncl.res.in/content/evaluation-adhesive-properties-vanillin-derived-polyhydroxy-urethanes02231nas a2200229 4500008004100000022001400041245010100055210006900156260000900225300001200234490000600246520145100252653001601703653002501719653003101744653001901775653001301794100002301807700002201830700001701852856013201869 2026 eng d a2637-610500aRecyclable l-glutamic acid-based polyester schiff base cross-linker for 3D printing applications0 aRecyclable lglutamic acidbased polyester schiff base crosslinker cJAN  a641-6500 v83 a

An l-amino acid-based polyester Schiff base cross-linker was developed from amine-functionalized polyester and biobased methacrylate vanillin. Vanillin, one of the few biobased and aromatic compounds readily available on an industrial scale, has recently garnered significant attention from the polymer community. The l-amino acid-based polyester Schiff base cross-linker (P3) was synthesized by condensing the aldehyde group of methacrylate vanillin with the amine group of the l-glutamic acid polyester. This polymeric cross-linker was used in resin formulations consisting of isobornyl acrylate as a reactive diluent and diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide as the photoinitiator for digital light processing (DLP) three-dimensional (3D) printing. The resulting 3D-printed parts exhibited good mechanical properties, with a Young's modulus of 1.5 GPa, and high thermal stability, with a T max of 410 degrees C. The chemical degradability of the 3D-printed materials was demonstrated in a mixture of tetrahydrofuran and diethylene triamine (1:1) at 80 degrees C for 48 h. The reusability of the recovered resin was demonstrated by adding fresh methacrylate vanillin and photoinitiator, followed by 3D printing using a DLP 3D printer. The 3D-printed parts produced from the recycled resin retained substantial mechanical properties, with a Young's modulus of 1.39 GPa, and thermal stability, with a T max of 390 degrees C.

10a3D printing10achemical degradation10acovalent adaptable network10al-glutamicacid10aVanillin1 aKamble, Ganesh, N.1 aGhute, Aaditi, P.1 aAsha, S., K. uhttps://library.ncl.res.in/content/recyclable-l-glutamic-acid-based-polyester-schiff-base-cross-linker-3d-printing-applications02655nas a2200289 4500008004100000022001400041245008500055210006900140260000800209490000800217520171400225653001601939653003101955653002201986653001602008653001302024100002902037700002502066700001802091700002302109700002002132700002202152700002302174700003102197700001702228856012002245 2026 eng d a1022-135200aVanillin-based recyclable thermosets and their glass fiber reinforced composites0 aVanillinbased recyclable thermosets and their glass fiber reinfo cJAN0 v2273 a

The accumulation of end-of-life plastic materials and composite reinforcement waste materials has brought much attention to developing sustainable alternatives and their re-processability. Incorporating covalent adaptable networks (CANs) into the crosslinked network bridges the concept of reversibility into the otherwise conventional non-reversible networks. This study investigates the structure-property relation in two reversible hardener systems derived from vanillin using Schiff base chemistry. The ``CAN'' systems were synthesized by condensation of vanillin with two amines, 4,4'-oxydianiline and tris(2-aminoethyl)amine, respectively, to form Va_ODA and Va_TAEA. The epoxy thermosets exhibited glass transition temperatures (T-g) of 125 degrees C and 115 degrees C, respectively, for Va_ODA and Va_TAEA, which is superior to most reversible vanillin-based systems reported. The vitrimer-thermosets exhibited promising mechanical and thermal properties, and reshaping abilities as a function of applied temperatures, indicating the dynamic nature of linkages. Chemical degradability was demonstrated by heating to 80 degrees C for 12 h in aqueous acidic medium or excess amine. The fabricated glass fiber composites exhibited good mechanical properties with tensile strength of 361 MPa and degradability in acetic acid/water mixture with a fiber recovery of >98 %. The recovered glass fiber exhibited almost similar tensile strength as the virgin glass fiber, demonstrating its potential reusability. The epoxy vitrimers underwent mechanical reprocessing through hot-pressing, as well as chemical reprocessing via 3D printing and by regeneration of imine bonds to form an epoxy resin.

10a3D printing10acovalent adaptable network10are-processability10aSchiff base10aVanillin1 aVeetil, Ashwani, Puthiya1 aRavikumar, Aniruddha1 aRajput, Tejas1 aSingh, Aman, Kumar1 aThakur, Tamanna1 aKrishna, Abhijith1 aPol, Harshawardhan1 aShanmuganathan, Kadhiravan1 aAsha, S., K. uhttps://library.ncl.res.in/content/vanillin-based-recyclable-thermosets-and-their-glass-fiber-reinforced-composites