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click chemistry (74) 74
chemistry, multidisciplinary (38) 38
chemistry (26) 26
click-chemie (24) 24
index medicus (24) 24
cycloaddition (22) 22
chemistry, organic (21) 21
click-chemistry (20) 20
alkynes (19) 19
azides (18) 18
organic chemistry (17) 17
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analysis (14) 14
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copper (12) 12
silylation (12) 12
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complexes (11) 11
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chemistry, inorganic & nuclear (10) 10
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azid (8) 8
cellulose (8) 8
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triazole (8) 8
1,3-dipolar cycloadditions (7) 7
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acids (6) 6
azide (6) 6
azide-alkyne cycloaddition (6) 6
chemical properties (6) 6
chemical reactions (6) 6
functionalisation (6) 6
kupfer (6) 6
ligands (6) 6
monomers (6) 6
peptides (6) 6
polysaccharides (6) 6
silatrane (6) 6
silica (6) 6
silylierung (6) 6
surface modification (6) 6
thiols (6) 6
transfer radical polymerization (6) 6
amino acids (5) 5
azides - chemistry (5) 5
biochemistry & molecular biology (5) 5
block-copolymers (5) 5
chemical sciences (5) 5
click reaction (5) 5
efficient (5) 5
elementaranalyse (5) 5
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humans (5) 5
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triethoxysilane (5) 5
1,2,3-triazole (4) 4
amines (4) 4
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antibacterial agents (4) 4
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chemistry, analytical (4) 4
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click (4) 4
conjugation (4) 4
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fluoride (4) 4
fluorides (4) 4
fourier transforms (4) 4
fourier-transform-infrared-spectroscopy (4) 4
ftir-spektroskopie (4) 4
functionalization (4) 4
gels (4) 4
graphene (4) 4
heterogeneous catalysis (4) 4
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Tetrahedron Letters, ISSN 0040-4039, 01/2014, Volume 55, Issue 4, pp. 903 - 909
The copper-catalyzed ‘click silylation’ has been exploited for the chemical modification of γ-azidopropyltriethoxysilane (AzPTES) with a wide range of terminal... 
Functional alkyne | CuBr(PPh3)3 | Heterocycle | Triethoxysilane | Click silylation | CuBr(PPh | POLYMERS | ALDEHYDE | HYDROGENATION | ANALOGS | SURFACE MODIFICATION | CHEMISTRY, ORGANIC | GAS-PHASE | CuBr(PPh3) | DERIVATIVES | Synthesis (chemistry) | Tetrahedrons | Infrared radiation | Spectra | Terminals | Derivatives | Nuclear magnetic resonance | Alkynes
Journal Article
Journal of Molecular Structure, ISSN 0022-2860, 01/2015, Volume 1079, pp. 173 - 181
Modified Schiff base silatranes (4a–4d) derived from novel terminal alkynes (2a–2d) were synthesized and fully characterized by IR, NMR (1H, 13C), mass... 
Schiff base | Terminal alkyne | Triethoxysilane | Silatrane | Click Silylation | Click | Silylation | LIGAND SYNTHESIS | ROUTE | AZIDES | COMPLEXES | REACTIVITY | LIGATION | CHEMISTRY, PHYSICAL | STRUCTURAL-CHARACTERIZATION | CHEMISTRY | PENTACOORDINATE | EFFICIENT | Schiff bases | Analysis | Chemical properties | Triazoles | Mass spectrometry | Capping | Diffraction | X-rays | Triethanolamine | Mass spectroscopy | Terminals | Alkynes
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 04/2014, Volume 55, Issue 15, pp. 2551 - 2558
A series of substituted aniline derivatized bis(1,2,3-triazolyl-γ-propylsilatranes) 3a–3f were designed in good yield from their triethoxysilane analogues via... 
Fluorescence | Hydrolysis study | Cu(PPh3)3Br | Cu2+ sensing | Click Silylation | Bis-silatrane | AZIDE-ALKYNE CYCLOADDITION | ANALOGS | STRATEGY | LOADINGS | CHEMISTRY, ORGANIC | Cu(PPh3)Br | AFFINITY | ALUMATRANE | CHEMISTRY | SILICA | DERIVATIVES | SILATRANE
Journal Article
Journal of Organometallic Chemistry, ISSN 0022-328X, 10/2014, Volume 769, pp. 124 - 129
A single step reaction for the synthesis of novel 1,2,3-triazole based silatranes (TBS)-scaffolds (2a–2o) using polyfunctionalised organotriethoxysilanes... 
Trisalkoxyamine | 1,2,3-Triazole | Click silylation | Triethoxysilane | Silatrane | SILICON | STEREOCHEMISTRY | SURFACE MODIFICATION | REACTIVITY | CHEMISTRY, ORGANIC | AZIDE | MOLECULES | CHEMISTRY, INORGANIC & NUCLEAR | FUNCTIONALIZATION | CHEMISTRY | PENTACOORDINATE | Triazoles
Journal Article
Organic Letters, ISSN 1523-7060, 03/2011, Volume 13, Issue 5, pp. 1102 - 1105
A structurally well-defined copper(I) isonitrile complex is shown to be an efficient, heterogeneous catalyst for the Huisgen azide−alkyne 1,3-dipolar... 
1,3-DIPOLAR CYCLOADDITIONS | HUISGEN CYCLOADDITION | BIS-SILYLATION | LIGANDS | ISOCYANIDE | TRIAZOLE | CLICK CHEMISTRY | POLYMER | REACTIVITY | LIGATION | CHEMISTRY, ORGANIC
Journal Article
Carbohydrate Polymers, ISSN 0144-8617, 02/2019, Volume 206, pp. 174 - 178
•One-pot synthesis of regioselectivly brominated and silylated cellulose.•Nucleophilic substitution on organosoluble cellulose... 
Click chemistry | Azide | Bromination | Huisgen cycloaddition | Cellulose | POLYMER SCIENCE | POLYSACCHARIDES | CHEMISTRY | CHEMISTRY, ORGANIC | CHEMISTRY, APPLIED | DERIVATIVES | Nuclear magnetic resonance spectroscopy | Analysis
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 06/2012, Volume 50, Issue 12, pp. 2319 - 2329
Amphiphilic polymers have recently garnered much attention due to their potential use in drug delivery and other biomedical applications. A modular synthesis... 
click chemistry | triblock copolymers | self‐assembly | self-assembly | DRUG | POLYMERS | POLYMER SCIENCE | POLY(2-OXAZOLINE)S | COMPLEXES | CHEMISTRY | BLOCK | POLYSILOXANE | Triblock copolymers
Journal Article
Journal of Organometallic Chemistry, ISSN 0022-328X, 09/2018, Volume 871, pp. 21 - 27
A single step Cu (I) assisted click silylation reaction had been used for the synthesis of novel Schiff based 1,2,3-triazole bridged silatrane... 
Triazole | Antibacterial | Click silylation | Silatrane | Trialkoxysilane | CLICK CHEMISTRY | COMPLEXES | CHEMISTRY, ORGANIC | SURFACES | CHEMISTRY, INORGANIC & NUCLEAR | Triazoles | Antibacterial agents | Analysis
Journal Article
Tetrahedron, ISSN 0040-4020, 03/2017, Volume 73, Issue 12, pp. 1529 - 1533
CO2 capture and release behaviors of three amidines bearing silatranyl group in DMSO solution were evaluated under dry conditions containing a very small... 
Amidine | Silatrane | Capture | Release | Carbon dioxide | POLYMERS | GELS | CHEMISTRY, ORGANIC | EMULSION POLYMERIZATION | MOIETIES | SURFACTANT | MATRICES | CHEMISTRY | CLICK SILYLATION | FIXATION-RELEASE SYSTEM | CARBON-DIOXIDE
Journal Article
RSC ADVANCES, ISSN 2046-2069, 2018, Volume 8, Issue 64, pp. 36445 - 36452
This report demonstrates the mimicking of an electronic circuit diagram towards Ce(iii) ion sensing response supported by molecular keypads. The probe naphthyl... 
CU2 | DESIGN | CHEMOSENSORS | FLUORESCENT SENSOR | CERIUM(III) IONS | CHEMISTRY | FRAMEWORK | SCHIFF-BASE | CLICK SILYLATION | METAL-IONS | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Inorganic Chemistry Communications, ISSN 1387-7003, 02/2018, Volume 88, pp. 11 - 20
The review essentially highlights the chronological development in organosilicon chemistry. The versatile application of silicon in organic, coordination,... 
Organosilicon | Click silylation | Higher coordinate silicon | Silatranes | TRANSANNULAR INTERACTION | MOLECULAR-STRUCTURE | HYDROSILYLATION | SILATRANE DERIVATIVES | CRYSTAL-STRUCTURES | CHEMISTRY, INORGANIC & NUCLEAR | N-METHYL | PENTACOORDINATE SILICON | ALUMATRANE | TRIS(2-HYDROXYETHYL)AMINE | SOL-GEL PROCESS | Silicon | Silane
Journal Article
RSC Advances, ISSN 2046-2069, 07/2015, Volume 5, Issue 81, pp. 65963 - 65974
This work presents the design, synthesis, UV-Vis absorption properties and Cu2+ ion binding of the organo-silicon complexes (3a-h) with different coordination... 
TURN-ON | TRANSITION-METAL IONS | RECOGNITION | CHEMOSENSORS | FLUORESCENT SENSOR | COMPLEXES | CLICK SILYLATION | MESOPOROUS SILICA | CHEMISTRY, MULTIDISCIPLINARY | AQUEOUS-SOLUTION | SILATRANE
Journal Article