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chemistry (11) 11
polymer science (11) 11
polymers (11) 11
1,3-dipolar cycloaddition (8) 8
click chemistry (8) 8
facile synthesis (8) 8
alkynes (7) 7
free click polymerization (7) 7
metal-free (7) 7
polymerization (7) 7
1,3-dipolar polycycloaddition (6) 6
polymer (6) 6
alkine (5) 5
azide-alkyne cycloaddition (5) 5
polymers - chemistry (5) 5
1,3-dipolar cycloadditions (4) 4
aggregation-enhanced emission (4) 4
aggregation-induced emission (4) 4
azid (4) 4
azides - chemistry (4) 4
chemistry, multidisciplinary (4) 4
cycloaddition (4) 4
emission (4) 4
molecular structure (4) 4
polymerisation (4) 4
terminal alkynes (4) 4
alkynes - chemistry (3) 3
azides (3) 3
catalysis (3) 3
catalyzed cycloaddition (3) 3
chemistry, organic (3) 3
explosives (3) 3
hyperbranched polymers (3) 3
hyperbranched polytriazoles (3) 3
polymers - chemical synthesis (3) 3
polys (3) 3
quenching (3) 3
sensors (3) 3
triazoles - chemical synthesis (3) 3
triazoles - chemistry (3) 3
1,3‐dipolar cycloaddition (2) 2
1,3‐dipolar polycycloaddition (2) 2
3-dipolar cycloaddition (2) 2
3-dipolar polycycloaddition (2) 2
ab monomers (2) 2
activated azide (2) 2
application (2) 2
azide (2) 2
chemosensor (2) 2
click polymerization (2) 2
click-chemie (2) 2
click-chemistry (2) 2
cross-linking (2) 2
cycloaddition reaction (2) 2
derivatives (2) 2
efficient (2) 2
enhanced emission (2) 2
explosives detection (2) 2
fluorescence (2) 2
internal alkynes (2) 2
material-science (2) 2
molekulargewicht (2) 2
nitrile oxides (2) 2
photonic properties (2) 2
polycyclotrimerization (2) 2
polymer industry (2) 2
polytriazoles (2) 2
reaction-condition (2) 2
reaktionsbedingung (2) 2
regioselectivity (2) 2
regioselektivität (2) 2
solid-phase (2) 2
solvent (2) 2
thiol-yne chemistry (2) 2
werkstoffkunde (2) 2
zykloaddition (2) 2
1, 3-dipolar polycycloaddition (1) 1
1, 3‐dipolar polycycloaddition (1) 1
1,3-dicarbonyl compounds (1) 1
acrylamid (1) 1
activated (1) 1
activation energy (1) 1
activation-energy (1) 1
active internal alkyne (1) 1
addition-reactions (1) 1
aggregates (1) 1
aggregation‐enhanced emission (1) 1
aggregation‐induced emission (1) 1
airline security (1) 1
aktivierungsenergie (1) 1
alkene (1) 1
allyl compounds (1) 1
amination (1) 1
analysis (1) 1
animal behavior (1) 1
auroras (1) 1
baugruppe (1) 1
benzotriazoles (1) 1
biochemistry & molecular biology (1) 1
bioconjugates (1) 1
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Polymer chemistry, ISSN 1759-9954, 2019, Volume 10, Issue 31, pp. 4271 - 4278
An efficient benzyne–azide polycycloaddition is established and functional poly(benzotriazole)s are produced under mild reaction conditions... 
BENZOTRIAZOLES | POLYTRIAZOLES | POLYMER SCIENCE | FREE CLICK POLYMERIZATION | HYPERBRANCHED POLYMERS | AGGREGATION-INDUCED EMISSION | 1,3-DIPOLAR CYCLOADDITION | CHEMISTRY | STRAIN | DERIVATIVES | METAL-FREE
Journal Article
Macromolecular rapid communications., ISSN 1022-1336, 2012, Volume 33, Issue 16, pp. 1356 - 1361
Journal Article
Journal Article
CHEMICAL SCIENCE, ISSN 2041-6520, 2016, Volume 7, Issue 10, pp. 6298 - 6308
Given the wide utility of click-chemistry reactions for the preparation of simple moieties within large architecturally complex materials, this minireview... 
LIGHT-EMITTING-DIODES | AZIDE-ALKYNE CYCLOADDITION | 1,3-DIPOLAR POLYCYCLOADDITION | MOLECULAR WIRES | AGGREGATION-ENHANCED EMISSION | TERMINAL ALKYNES | CHEMICAL-BIOLOGY | HETEROJUNCTION SOLAR-CELLS | CHEMISTRY, MULTIDISCIPLINARY | METAL-FREE | POLY(VINYLENE SULFIDE)S | Electronics | Paper | Utilities | Surveying | Polymers
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 11/2000, Volume 2000, Issue 22, pp. 3659 - 3673
Microwave irradiation has been applied with success to cycloaddition reactions. The special characteristics of such irradiation entails the use of new... 
Fullerenes | Microwave | Heterocycles | Cycloadditions | Natural products | INDUCED 1,3-DIPOLAR CYCLOADDITION | CHEMISTRY, ORGANIC | cycloadditions | fullerenes | SOLVENT | natural products | heterocycles | ORGANIC-REACTION ENHANCEMENT | NITRILE OXIDES | DIELS-ALDER REACTION | ADDITION-REACTIONS | CHEMISTRY | C-60 | RAPID SYNTHESIS | microwave | DRY MEDIA
Journal Article
JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, ISSN 0037-9980, 09/2016, Volume 74, Issue 9, pp. 866 - 876
This review describes the development of nitrile N-oxide-based click agents to fabricate multi component organic architectures. Central to the technique to... 
1,3-DIPOLAR CYCLOADDITIONS | click reaction | nitrile N-oxide | dearomatization | grafting | NUCLEAR-MAGNETIC-RESONANCE | CHEMISTRY, ORGANIC | POLYMERIZATION | SOLVENT | molecular integration | C-13-label | cycloaddition | cross-linking | kinetic stabilization | RING | dynamic character | CHEMISTRY | POLYROTAXANE | RADICALS | ISOCYANATES | DERIVATIVES
Journal Article