Research graph
References from Preparation of Bisfuran-Based Biopolythioureas via Multicomponent Polymerization and Its Performances as Biosorbent for Hg2+ Removal. Local targets link to admitted publications; unresolved targets remain external evidence.
Earth: An oxidative planet with limited atom resources and rich chemistry
10.1002/anie.202416459 · 2025 · External reference
Ensuring consistency between biogeochemical planetary boundaries
10.1038/s41893-026-01770-6 · 2026 · External reference
Synthesis of bisfuran-based long-chain biopolyamide ionomers through postpolymerization modification
10.1021/acsapm.5c02826 · 2025 · External reference
Polymerizations with elemental sulfur: from petroleum refining to polymeric materials
10.1021/jacs.1c09329 · 2022 · External reference
Room temperature one-step conversion from elemental sulfur to functional polythioureas through catalyst-free multicomponent polymerizations
10.1021/jacs.8b02886 · 2018 · External reference
Recent breakthroughs in deep aerobic oxidative desulfurization of petroleum refinery products
10.1016/j.jclepro.2020.125731 · 2021 · External reference
Recent advances of gaseous pollutant catalytic oxidation over precious metal catalysts with SO2 exposure
10.1021/acs.est.4c13228 · 2025 · External reference
Turning two waste streams into one solution for enhancing sustainability of the built environment
10.1016/j.resconrec.2021.105778 · 2021 · External reference
The use of elemental sulfur as an alternative feedstock for polymeric materials
10.1038/nchem.1624 · 2013 · External reference
Recent advances in organic reactions involving elemental sulfur
10.1002/adsc.201601329 · 2017 · External reference
Three-component reaction between alkynes, elemental sulfur, and aliphatic amines: a general, straightforward, and atom economical approach to thioamides
10.1021/ol403345e · 2014 · External reference
Biomass-based polyureas derived from rigid furfurylamine and isomannide
10.1021/acsapm.2c00204 · 2022 · External reference
A novel amine-first strategy suitable for preparing both functional and engineering bio-polyamides: furfurylamine as the sole furan source for bisfuranic diamine/diacid monomers
10.1039/d4py00567h · 2024 · External reference
Synthesis and Characterization of Novel Biobased Ion-Exchange Bisfuran Polyamides Prepared by Interfacial Polycondensation of Bisfuran Diamine Monomer and Sustainable Dicarboxylic Acid Derivatives
10.1007/s10924-022-02496-0 · 2022 · External reference
A novel bio-based AB2 monomer for preparing hyperbranched polyamides derived from levulinic acid and furfurylamine
10.1039/c9py01253b · 2019 · External reference
Synthesis and Hg2+ removal ability of renewable furfurylamine-derived bio-polythioureas
10.1016/j.eurpolymj.2024.113144 · 2024 · External reference
The base-free multicomponent polymerization of elemental sulfur, difluoromethylene phosphobetaine and amines toward electron-deficient aromatic polythioureas
10.1039/d4py01387e · 2025 · External reference
Fluorescent and magnetic mesoporous hybrid material: A chemical and biological nanosensor for Hg2+ ions
10.1038/srep21820 · 2016 · External reference
Superior removal of Hg (II) ions from wastewater using hierarchically porous, functionalized carbon
10.1016/j.jhazmat.2019.02.099 · 2019 · External reference
High-efficient and superfast capture of Hg2+, Pb2+, and Ag+ ions from wastewater using ethylenediamine intercalated MoSe2 nanoflowers
10.1016/j.jhazmat.2025.139435 · 2025 · External reference
Switchable and highly selective Hg(II) capture enabled by a thermo-responsive MOF-polymer nanohybrid
10.1016/j.cej.2025.166826 · 2025 · External reference
Spontaneous bio-derived porous hydrogels for sustainable pollutant removal from contaminated water
10.1002/adfm.202519401 · 2026 · External reference
Recent advances in waste-derived functional materials for wastewater remediation
10.1016/j.eehl.2022.05.001 · 2022 · External reference
Absolute hardness: companion parameter to absolute electronegativity
10.1021/ja00364a005 · 1983 · External reference
Removal of Hg(II) ions from aqueous solution by poly(allylamine-co-methacrylamide-co-dimethylthiourea)
10.1016/j.jiec.2019.12.023 · 2020 · External reference
Multicomponent polymerizations of elemental sulfur, CH2Cl2, and aromatic amines toward chemically recyclable functional aromatic polythioureas
10.1021/jacs.4c02155 · 2024 · External reference
Newly developed multicomponent polycondensation involving sulfur for the successful synthesis of biobased polythioureas
10.1021/acs.macromol.5c00177 · 2025 · External reference
A Sequential Ugi Multicomponent/Cu-Catalyzed Azide–Alkyne Cycloaddition Approach for the Continuous Flow Generation of Cyclic Peptoids
10.1021/acs.joc.5b00445 · 2015 · External reference
Enhancing the scope of the Diels–Alder reaction through isonitrile chemistry: Emergence of a new class of acyl-activated dienophiles
10.1021/ja303876e · 2012 · External reference
Endo and exo Diels–Alder Adducts: Temperature-tunable building blocks for selective chemical functionalization
10.1021/jacs.8b01544 · 2018 · External reference
Multicomponent polymerization of sulfur, chloroform and diamine toward polythiourea
10.1007/s11426-022-1483-8 · 2023 · External reference
Synthesis of furan-based cationic biopolyamides and their removal abilities for perfluoroalkyl and polyfluoroalkyl substances
10.1016/j.cej.2025.160306 · 2025 · External reference
Progress in isocyanide-based step-growth polymerization
10.1002/macp.202200352 · 2023 · External reference
Isoindolinone compounds active as Kv1.5 blockers identified using a multicomponent reaction approach
10.1016/j.bmcl.2016.02.081 · 2016 · External reference
A more sustainable and highly practicable synthesis of aliphatic isocyanides
10.1039/c9gc04070f · 2020 · External reference
First report on bio-catalytic N-formylation of amines using ethyl formate
10.1039/c6cc07679c · 2017 · External reference
Isonitrile alkylations: a rapid route to imidazo[1,5-a]pyridines
10.1039/c5cc08724d · 2016 · External reference
A rapid and efficient synthesis of symmetrical disulfides under microwave irradiation conditions
10.1081/scc-120003143 · 2002 · External reference
Metal- and solvent-free synthesis of substituted pyrimidines via an NH4I-promoted three-component tandem reaction
10.1021/acs.joc.3c01700 · 2023 · External reference
Copper-catalyzed thiocarbonylation and thiolation of alkyl iodides
10.1039/d2ob00008c · 2022 · External reference
Physical properties of poly(ether-thiourea)-based elastomer formed by zigzag hydrogen bonding and slidable cross-linking
10.1021/acsmacrolett.3c00526 · 2023 · External reference
Synthesis of sulfur nanoparticles in aqueous surfactant solutions
10.1016/j.jcis.2009.12.004 · 2010 · External reference
Polythiourea superionic conductors for solid-state batteries
10.1021/acs.macromol.3c00116 · 2023 · External reference
Reactivities and mechanisms in organic reactions involving activation of elemental sulfur under basic conditions
10.1016/j.tchem.2024.100086 · 2024 · External reference
Preparation of polythioamides from dialdehydes and diamines with sulfur by the Willgerodt–Kindler type reaction
10.1002/pola.10019 · 2001 · External reference
Understanding the reactivity of captodative ethylenes in polar cycloaddition reactions. A theoretical study
10.1021/jo800572a · 2008 · External reference
Electrophilicity index
10.1021/ja983494x · 1999 · External reference
Infrared spectra and structures of aniline+–furan and aniline+–phenol. Preference between π-type and σ-type hydrogen-bonded structures
10.1016/s0009-2614(03)00985-0 · 2003 · External reference
Study on ultrasonic assisted mechanism of ring opening polymerization of octamethylcyclotetrasiloxane (D4)
10.1063/1.5041098 · 2018 · External reference
Applications of ultrasound to materials chemistry
10.1146/annurev.matsci.29.1.295 · 1999 · External reference
Unveiling the “sono-physico-chemical” essence: Cavitation and vibration effects in ultrasound–assisted processes
10.1016/s1872-2067(24)60028-8 · 2024 · External reference
Synthesis of polyamides by energy-efficient ultrasonic-assisted direct polycondensation
10.1177/0954008311416525 · 2011 · External reference
Ultrasound in polymer chemistry: Revival of an established technique
10.1002/pola.21646 · 2006 · External reference
Comparison of cross-linked branched and linear poly(ethylene imine) microgel microstructures and their impact in antimicrobial behavior, copper chelation, and carbon dioxide capture
10.1021/acsapm.9b01101 · 2020 · External reference
The interplay between kinetics and thermodynamics in furan Diels–Alder chemistry for sustainable chemicals production
10.1002/anie.202114720 · 2022 · External reference
Low-temperature processable glass fiber reinforced aromatic diamine chain extended bismaleimide composites with improved mechanical properties
10.1002/pc.26760 · 2022 · External reference
Inverse vulcanization employing epoxy compounds as crosslinking agents for elemental sulfur in the preparation of sulfur-rich epoxy resins
10.1039/d4py00074a · 2024 · External reference
Manipulating cis-trans copolymer chain conformation to simultaneously improve permittivity and DC breakdown strength in polythiourea
10.1002/marc.202300501 · 2024 · External reference
Composite of aromatic polythiourea/BaTiO3 nanowires with high energy density and high discharge efficiency for energy storage applications
10.1007/s10854-021-06450-z · 2021 · External reference
Catalyst-free construction of versatile and functional CS2-based polythioureas: Characteristics from self-healing to heavy metal absorption
10.1021/acs.macromol.9b01811 · 2019 · External reference
the decomposition of thiourea in water solutions
10.1021/ja01603a014 · 1956 · External reference
Raman spectroscopic studies on the complexation and adsorbed behaviour of thiourea
1989 · External reference
Removal of Hg(II) with MgAl-layered double hydroxide functionalized by schiff base ligands: Application and condition optimization
10.1016/j.chemosphere.2024.142972 · 2024 · External reference
Sustainable removal of Hg(II) by sulfur-modified pine-needle biochar
10.1016/j.jhazmat.2020.122048 · 2020 · External reference
Different solvents accompanied by different structures: Catalyst-free one step construction of highly branched polythioureas and its properties
10.1016/j.eurpolymj.2024.113032 · 2024 · External reference
Removal of Cr6+ from aqueous solution using thiourea-glutaraldehyde double-crosslinked chitosan/sodium alginate composites
10.1111/wej.12976 · 2025 · External reference
Highly selective adsorption of mercury ions on nanocellulose-based polythiourea-modified composite aerogels
10.1016/j.seppur.2025.134905 · 2025 · External reference
Spontaneous bio-derived porous hydrogels for sustainable pollutant removal from contaminated water
10.1002/adfm.202519401 · ExternalCitation · doi-reference
Recent advances in organic reactions involving elemental sulfur
10.1002/adsc.201601329 · ExternalCitation · doi-reference
The interplay between kinetics and thermodynamics in furan Diels–Alder chemistry for sustainable chemicals production
10.1002/anie.202114720 · ExternalCitation · doi-reference
Earth: An oxidative planet with limited atom resources and rich chemistry
10.1002/anie.202416459 · ExternalCitation · doi-reference
Progress in isocyanide-based step-growth polymerization
10.1002/macp.202200352 · ExternalCitation · doi-reference
Manipulating cis-trans copolymer chain conformation to simultaneously improve permittivity and DC breakdown strength in polythiourea
10.1002/marc.202300501 · ExternalCitation · doi-reference
Low-temperature processable glass fiber reinforced aromatic diamine chain extended bismaleimide composites with improved mechanical properties
10.1002/pc.26760 · ExternalCitation · doi-reference
Preparation of polythioamides from dialdehydes and diamines with sulfur by the Willgerodt–Kindler type reaction
10.1002/pola.10019 · ExternalCitation · doi-reference
Ultrasound in polymer chemistry: Revival of an established technique
10.1002/pola.21646 · ExternalCitation · doi-reference
Composite of aromatic polythiourea/BaTiO3 nanowires with high energy density and high discharge efficiency for energy storage applications
10.1007/s10854-021-06450-z · ExternalCitation · doi-reference
Synthesis and Characterization of Novel Biobased Ion-Exchange Bisfuran Polyamides Prepared by Interfacial Polycondensation of Bisfuran Diamine Monomer and Sustainable Dicarboxylic Acid Derivatives
10.1007/s10924-022-02496-0 · ExternalCitation · doi-reference
Multicomponent polymerization of sulfur, chloroform and diamine toward polythiourea
10.1007/s11426-022-1483-8 · ExternalCitation · doi-reference
Isoindolinone compounds active as Kv1.5 blockers identified using a multicomponent reaction approach
10.1016/j.bmcl.2016.02.081 · ExternalCitation · doi-reference
Synthesis of furan-based cationic biopolyamides and their removal abilities for perfluoroalkyl and polyfluoroalkyl substances
10.1016/j.cej.2025.160306 · ExternalCitation · doi-reference
Switchable and highly selective Hg(II) capture enabled by a thermo-responsive MOF-polymer nanohybrid
10.1016/j.cej.2025.166826 · ExternalCitation · doi-reference
Removal of Hg(II) with MgAl-layered double hydroxide functionalized by schiff base ligands: Application and condition optimization
10.1016/j.chemosphere.2024.142972 · ExternalCitation · doi-reference
Recent advances in waste-derived functional materials for wastewater remediation
10.1016/j.eehl.2022.05.001 · ExternalCitation · doi-reference
Different solvents accompanied by different structures: Catalyst-free one step construction of highly branched polythioureas and its properties
10.1016/j.eurpolymj.2024.113032 · ExternalCitation · doi-reference
Synthesis and Hg2+ removal ability of renewable furfurylamine-derived bio-polythioureas
10.1016/j.eurpolymj.2024.113144 · ExternalCitation · doi-reference
Synthesis of sulfur nanoparticles in aqueous surfactant solutions
10.1016/j.jcis.2009.12.004 · ExternalCitation · doi-reference
Recent breakthroughs in deep aerobic oxidative desulfurization of petroleum refinery products
10.1016/j.jclepro.2020.125731 · ExternalCitation · doi-reference
Superior removal of Hg (II) ions from wastewater using hierarchically porous, functionalized carbon
10.1016/j.jhazmat.2019.02.099 · ExternalCitation · doi-reference
Sustainable removal of Hg(II) by sulfur-modified pine-needle biochar
10.1016/j.jhazmat.2020.122048 · ExternalCitation · doi-reference
High-efficient and superfast capture of Hg2+, Pb2+, and Ag+ ions from wastewater using ethylenediamine intercalated MoSe2 nanoflowers
10.1016/j.jhazmat.2025.139435 · ExternalCitation · doi-reference
Removal of Hg(II) ions from aqueous solution by poly(allylamine-co-methacrylamide-co-dimethylthiourea)
10.1016/j.jiec.2019.12.023 · ExternalCitation · doi-reference
Turning two waste streams into one solution for enhancing sustainability of the built environment
10.1016/j.resconrec.2021.105778 · ExternalCitation · doi-reference
Highly selective adsorption of mercury ions on nanocellulose-based polythiourea-modified composite aerogels
10.1016/j.seppur.2025.134905 · ExternalCitation · doi-reference
Reactivities and mechanisms in organic reactions involving activation of elemental sulfur under basic conditions
10.1016/j.tchem.2024.100086 · ExternalCitation · doi-reference
Infrared spectra and structures of aniline+–furan and aniline+–phenol. Preference between π-type and σ-type hydrogen-bonded structures
10.1016/s0009-2614(03)00985-0 · ExternalCitation · doi-reference
Unveiling the “sono-physico-chemical” essence: Cavitation and vibration effects in ultrasound–assisted processes
10.1016/s1872-2067(24)60028-8 · ExternalCitation · doi-reference
Recent advances of gaseous pollutant catalytic oxidation over precious metal catalysts with SO2 exposure
10.1021/acs.est.4c13228 · ExternalCitation · doi-reference
Metal- and solvent-free synthesis of substituted pyrimidines via an NH4I-promoted three-component tandem reaction
10.1021/acs.joc.3c01700 · ExternalCitation · doi-reference
A Sequential Ugi Multicomponent/Cu-Catalyzed Azide–Alkyne Cycloaddition Approach for the Continuous Flow Generation of Cyclic Peptoids
10.1021/acs.joc.5b00445 · ExternalCitation · doi-reference
Polythiourea superionic conductors for solid-state batteries
10.1021/acs.macromol.3c00116 · ExternalCitation · doi-reference
Newly developed multicomponent polycondensation involving sulfur for the successful synthesis of biobased polythioureas
10.1021/acs.macromol.5c00177 · ExternalCitation · doi-reference
Catalyst-free construction of versatile and functional CS2-based polythioureas: Characteristics from self-healing to heavy metal absorption
10.1021/acs.macromol.9b01811 · ExternalCitation · doi-reference
Biomass-based polyureas derived from rigid furfurylamine and isomannide
10.1021/acsapm.2c00204 · ExternalCitation · doi-reference
Synthesis of bisfuran-based long-chain biopolyamide ionomers through postpolymerization modification
10.1021/acsapm.5c02826 · ExternalCitation · doi-reference
Comparison of cross-linked branched and linear poly(ethylene imine) microgel microstructures and their impact in antimicrobial behavior, copper chelation, and carbon dioxide capture
10.1021/acsapm.9b01101 · ExternalCitation · doi-reference
Physical properties of poly(ether-thiourea)-based elastomer formed by zigzag hydrogen bonding and slidable cross-linking
10.1021/acsmacrolett.3c00526 · ExternalCitation · doi-reference
Absolute hardness: companion parameter to absolute electronegativity
10.1021/ja00364a005 · ExternalCitation · doi-reference
the decomposition of thiourea in water solutions
10.1021/ja01603a014 · ExternalCitation · doi-reference
Enhancing the scope of the Diels–Alder reaction through isonitrile chemistry: Emergence of a new class of acyl-activated dienophiles
10.1021/ja303876e · ExternalCitation · doi-reference
Electrophilicity index
10.1021/ja983494x · ExternalCitation · doi-reference
Polymerizations with elemental sulfur: from petroleum refining to polymeric materials
10.1021/jacs.1c09329 · ExternalCitation · doi-reference
Multicomponent polymerizations of elemental sulfur, CH2Cl2, and aromatic amines toward chemically recyclable functional aromatic polythioureas
10.1021/jacs.4c02155 · ExternalCitation · doi-reference
Endo and exo Diels–Alder Adducts: Temperature-tunable building blocks for selective chemical functionalization
10.1021/jacs.8b01544 · ExternalCitation · doi-reference
Room temperature one-step conversion from elemental sulfur to functional polythioureas through catalyst-free multicomponent polymerizations
10.1021/jacs.8b02886 · ExternalCitation · doi-reference
Understanding the reactivity of captodative ethylenes in polar cycloaddition reactions. A theoretical study
10.1021/jo800572a · ExternalCitation · doi-reference
Three-component reaction between alkynes, elemental sulfur, and aliphatic amines: a general, straightforward, and atom economical approach to thioamides
10.1021/ol403345e · ExternalCitation · doi-reference
The use of elemental sulfur as an alternative feedstock for polymeric materials
10.1038/nchem.1624 · ExternalCitation · doi-reference
Ensuring consistency between biogeochemical planetary boundaries
10.1038/s41893-026-01770-6 · ExternalCitation · doi-reference
Fluorescent and magnetic mesoporous hybrid material: A chemical and biological nanosensor for Hg2+ ions
10.1038/srep21820 · ExternalCitation · doi-reference
Isonitrile alkylations: a rapid route to imidazo[1,5-a]pyridines
10.1039/c5cc08724d · ExternalCitation · doi-reference
First report on bio-catalytic N-formylation of amines using ethyl formate
10.1039/c6cc07679c · ExternalCitation · doi-reference
A more sustainable and highly practicable synthesis of aliphatic isocyanides
10.1039/c9gc04070f · ExternalCitation · doi-reference
A novel bio-based AB2 monomer for preparing hyperbranched polyamides derived from levulinic acid and furfurylamine
10.1039/c9py01253b · ExternalCitation · doi-reference
Copper-catalyzed thiocarbonylation and thiolation of alkyl iodides
10.1039/d2ob00008c · ExternalCitation · doi-reference
Inverse vulcanization employing epoxy compounds as crosslinking agents for elemental sulfur in the preparation of sulfur-rich epoxy resins
10.1039/d4py00074a · ExternalCitation · doi-reference
A novel amine-first strategy suitable for preparing both functional and engineering bio-polyamides: furfurylamine as the sole furan source for bisfuranic diamine/diacid monomers
10.1039/d4py00567h · ExternalCitation · doi-reference
The base-free multicomponent polymerization of elemental sulfur, difluoromethylene phosphobetaine and amines toward electron-deficient aromatic polythioureas
10.1039/d4py01387e · ExternalCitation · doi-reference
Study on ultrasonic assisted mechanism of ring opening polymerization of octamethylcyclotetrasiloxane (D4)
10.1063/1.5041098 · ExternalCitation · doi-reference
A rapid and efficient synthesis of symmetrical disulfides under microwave irradiation conditions
10.1081/scc-120003143 · ExternalCitation · doi-reference
Removal of Cr6+ from aqueous solution using thiourea-glutaraldehyde double-crosslinked chitosan/sodium alginate composites
10.1111/wej.12976 · ExternalCitation · doi-reference
Applications of ultrasound to materials chemistry
10.1146/annurev.matsci.29.1.295 · ExternalCitation · doi-reference
Synthesis of polyamides by energy-efficient ultrasonic-assisted direct polycondensation
10.1177/0954008311416525 · ExternalCitation · doi-reference
