about
Hydrogen-Bonded Macrocyclic Supramolecular Systems in Solution and on SurfacesRecent advances in glycerol polymers: chemistry and biomedical applicationsOptically responsive supramolecular polymer glasses.Dynamic urea bond for the design of reversible and self-healing polymersMendable polymersSelective isolation of gold facilitated by second-sphere coordination with α-cyclodextrinSelf-healing polymers via supramolecular forces.Advancing Tissue Engineering: A Tale of Nano-, Micro-, and Macroscale Integration.Synthesis of doubly ethyl-bridged bis(p-sulfonatocalix[4]arene) and its supramolecular polymerization with viologen dimer.Block copolymer libraries: modular versatility of the macromolecular Lego system.Dynamic microfluidic control of supramolecular peptide self-assembly.Novel EDTA-ligands containing an integral perylene bisimide (PBI) core as an optical reporter unit.Multistimuli-responsive supramolecular assembly of cucurbituril/cyclodextrin pairs with an azobenzene-containing bispyridinium guest.Mechanistic control over morphology: self-assembly of a discotic amphiphile in water.Mechanosensitive self-replication driven by self-organization.Temperature sensitive supramolecular self assembly of per-6-PEO-β-cyclodextrin and α,ω-di-(adamantylethyl)poly(N-isopropylacrylamide) in water.Supramolecular organic frameworks: engineering periodicity in water through host-guest chemistry.A Phosphorescent Platinum(II) Bipyridyl Supramolecular Polymer Based on Quadruple Hydrogen Bonds.Stimuli-controlled self-assembly of diverse tubular aggregates from one single small monomer.Highly branched and loop-rich gels via formation of metal-organic cages linked by polymers.Controlling the growth and shape of chiral supramolecular polymers in water.A luminescent coordination polymer based on bisterpyridyl ligand containing o-carborane: two tunable emission modes.Supramolecular Interfacial Polymerization: A Controllable Method of Fabricating Supramolecular Polymeric MaterialsSelf-assembly of "patchy" nanoparticles: a versatile approach to functional hierarchical materials.Thermoresponsive supramolecular dendronized polymers.Hierarchical formation of fibrillar and lamellar self-assemblies from guanosine-based motifsFacile synthesis of supramolecular ionic polymers that combine unique rheological, ionic conductivity, and self-healing properties.Dynamers: polyacylhydrazone reversible covalent polymers, component exchange, and constitutional diversityOrganic photonics: prospective nano/micro scale passive organic optical waveguides obtained from π-conjugated ligand molecules.Bis(4-fluoro-anilinium) sulfate.Chemoresponsive alternating supramolecular copolymers created from heterocomplementary calix[4]pyrrolesOlefin metathesis and quadruple hydrogen bonding: a powerful combination in multistep supramolecular synthesis.Recent developments in the supramolecular chemistry of terpyridine-metal complexes.Adaptable hydrogel networks with reversible linkages for tissue engineering.Exploiting Co-solubilization of Warfarin, Curcumin, and Rhodamine B for Modulation of Energy Transfer: A Micelle FRET On/Off Switch.Photoregulated release of noncovalent guests from dendritic amphiphilic nanocontainers.Tuning the nature and stability of self-assemblies formed by ester benzene 1,3,5-tricarboxamides: the crucial role played by the substituents.Dual hydrogen-bonding motifs in complexes formed between tropolone and formic acid.Biopolymers and supramolecular polymers as biomaterials for biomedical applications.3,5-Dimeth-oxy-4'-methyl-biphen-yl
P2860
Q26745716-0A87EFD5-DFC8-4047-861F-CD56C07A83A1Q26822786-E91D9D35-85F7-4EA4-87B2-E6EA29D3B933Q27324078-79F820EE-305C-4675-8950-CF15F514F109Q28307196-036AB58F-5E61-4F5E-A5A9-70137C3FEE19Q29012015-F7C111FE-8B26-42C3-8DB6-E3508CE435E2Q30051480-0C5304CE-CD80-4B6C-8341-724B0C6E988EQ30317905-6E928F01-52EC-47E8-9330-E15D4D22231DQ30358039-CE64D213-1071-4D84-8AB6-F95075E920B0Q30765822-76BBDE8F-F4E2-4227-989A-BD95798FE4FDQ30774396-661F24BE-0FB9-4FA5-B23C-EB529F8C6AFAQ30827291-EF6AA7FB-803D-4DCD-9FE8-F57E4A443164Q30839569-EC47630C-2D45-416B-A316-DA0BB9143920Q30857456-D863407E-A1EC-40DC-90AD-B8E8F9832DBCQ30867014-46D53486-8376-4E54-81A8-9E58E8D9C362Q30979826-BEA5FCCC-06AD-4737-B92B-AAB45F824590Q30980802-78FD2EB0-A46C-49FD-9E7F-80A8C7B0D726Q31081020-1EC19BDC-3427-4442-98DE-827D40C47A0DQ31139696-28D12FB4-32BC-4842-A691-F266051DA0B7Q33571985-F1F3F975-F81C-4CFD-BD1E-672ED0499C34Q33641117-7EB34120-A26E-4156-B649-BA919A2BAD85Q33710453-5113E6EE-1739-4D28-A7A0-971726784E50Q33801095-00453E3B-A80F-42DD-87A8-0CF54B2B551AQ33845891-0BAB7C83-D48E-492F-937A-4CB35F313CF5Q33868471-996BB12B-47A9-43AF-B531-2DF9D11B62AAQ34014745-F9C80D84-69DF-4AAB-B51D-11CBCA53A797Q34078690-61AFEEA6-E001-4167-B20C-4BA931DC4DC1Q34133810-326C9046-F879-4031-A513-62775BEB6005Q34374394-96D7C2BC-13C6-48F3-830B-683D4BF65E63Q35119257-2CEB47E6-5699-4445-A5D3-3605B0028E2CQ35438196-CF2C2B27-40EA-45EE-8C89-C4AEC2CF2AF9Q35641479-40CCFB58-355F-4CB4-92EE-36AF44A76F40Q35699965-D4097245-306F-4A96-8A3A-782CEBA591AFQ35849243-167C72E4-50A9-4970-B742-3306FE579DD2Q35927889-832853B6-5439-4EA2-97A0-215D37A27EC8Q36001587-4FBF89DE-3894-4A59-AAEA-8BF5CF22AC48Q36107250-8A58F22B-3EC7-4F19-9353-ECDFE124E05CQ36158981-8512C24F-EED1-472F-A0F0-3B981DFDE25EQ36210602-11A2C89E-FA0B-4356-BFD7-3CDD70178611Q36683929-C928208B-A8C3-4A9E-BA2F-F50ABE5FD6FAQ36775664-77D65A2E-2CA5-4F4D-99EE-D845187CAA20
P2860
description
im Dezember 2001 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 01 December 2001
@en
наукова стаття, опублікована в грудні 2001
@uk
name
Supramolecular Polymers
@en
type
label
Supramolecular Polymers
@en
prefLabel
Supramolecular Polymers
@en
P2093
P356
P1433
P1476
Supramolecular polymers
@en
P2093
B J Folmer
E W Meijer
L Brunsveld
R P Sijbesma
P304
P356
10.1021/CR990125Q
P50
P577
2001-12-01T00:00:00Z