Search results for "Pram"

showing 10 items of 1064 documents

Stabilisation of Exotic Tribromide (Br3−) Anions via Supramolecular Interaction with A Tosylated Macrocyclic Pyridinophane. A Serendipitous Case.

2020

Tetraaza-macrocyclic pyridinophane L-Ts, decorated with a p-toluenesulfonyl (tosyl

crystal structureStackingSupramolecular chemistryPharmaceutical ScienceCrystal structureAnalytical Chemistrylcsh:QD241-441symbols.namesakechemistry.chemical_compoundlcsh:Organic chemistryTosylDrug DiscoveryPyridineHirshfeld surface analysisPhysical and Theoretical ChemistryN-heterocyclesanion- interactionsTribromideHydrogen bondOrganic Chemistryanion complexesCrystallographychemistryChemistry (miscellaneous)symbolsMolecular Medicinevan der Waals forceMolecules
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Host-guest complexes of C-propyl-2-bromoresorcinarene with aromatic N-oxides*

2018

The host-guest complexes of C-propyl-2-bromoresorcinarene with pyridine N-oxide, 3-methylpyridine N-oxide, quinoline N-oxide and isoquinoline N-oxide are studied using single crystal X-ray crystallography and 1H NMR spectroscopy. The C-propyl-2-bromoresorcinarene forms endo-complexes with the aromatic N-oxides in the solid-state when crystallised from either methanol or acetone. In solution, the endo-complexes were observed only in methanol-d4. In DMSO the solvent itself is a good guest, and crystallisation provides only solvate endo-complexes. The C-propyl-2-bromoresorcinarene shows remarkable flexibility when crystallised from either methanol or acetone, and packs into one-dimensional sel…

crystal structurekemiaSupramolecular chemistryCrystal structurechemistry010402 general chemistry01 natural scienceschemistry.chemical_compoundPolymer chemistryPyridinecrystalssupramolekulaarinen kemiaAcetoneresorcinarenesmoleculesIsoquinolineta116Biochemistry Biophysics and Structural Biologyvetysidoksetta114010405 organic chemistryHydrogen bondQuinolinemolekyylitGeneral Chemistrykiteet0104 chemical sciencesaromatic N-oxidesSolventChemistrychemistryvetyhydrogenhydrogen bondsSupramolecular chemistrySUPRAMOLECULAR CHEMISTRY
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Spontaneous Resolution of an Electron‐Deficient Tetrahedral Fe4L4cage

2015

A highly electron-deficient C3-symmetric tris(bipyridyl) ligand was prepared in four steps and used for the coordination of Fe(OTf)2, thereby resulting in the homochiral assembly of a new family of robust tetrahedral M4L4 cages. This homochiral T-symmetric cage containing a relatively large cavity of 330 A(3) is capable of encapsulating an anionic guest, as was determined by mass spectrometry, (19)F NMR spectroscopy, and finally shown from its crystal structure. Moreover, crystallization of the cage from CH3CN led to crystals containing both (ΔΔΔΔ and ΛΛΛΛ) enantiomers, while crystallization from CH3 OH resulted in crystals containing only the right-handed (ΔΔΔΔ) cage. The difference in the…

crystallization010405 organic chemistryChemistryLigandelectron-deficient tetrahedral Fe4L4Supramolecular chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyCrystal structureGeneral Medicine010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceslaw.inventionCrystalCrystallographylawX-ray crystallographyCrystallizationChirality (chemistry)ta116Angewandte Chemie
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Nanodispositivi e macchine molecolari

2015

didattica nanoscienze chimica supramolecolare
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Nanodispositivi e macchine molecolari. Dai materiali alle scienze della vita

2015

didattica nanoscienze dispositivi molecolari chimica supramolecolare
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Efficient photoinduced electron transfer in a porphyrin tripod-fullerene supramolecular complex via pi-pi interactions in nonpolar media.

2010

A novel porphyrin tripod (TPZn(3)) was synthesized via "click chemistry". Three porphyrin moieties of TPZn(3) are geometrically close and linked by a flexible linker. The electron-transfer oxidation of TPZn(3) results in intramolecular pi-dimer formation between porphyrin moieties as indicated by electrochemical, vis-NIR, and ESR measurements. The cyclic voltammogram of TPZn(3) exhibited stepwise one-electron oxidation processes of three porphyrin moieties in the range from 0.58 to 0.73 V (vs SCE in CH(2)Cl(2)). When TPZn(3) was oxidized by tris(2,2'-bipyridyl)-ruthenium(III) ([Ru(bpy)(3)](3+)), the oxidized species (TPZn(3))(n+) (0n/= 3) exhibited a charge resonance band in the NIR region …

dyadFullerenePorphyrinsMacromolecular SubstancesPhotochemistrySupramolecular chemistrycharge-separated state010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCatalysisPhotoinduced electron transferchemistry.chemical_compoundColloid and Surface Chemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistryMoleculeComputingMilieux_MISCELLANEOUSMolecular Structure[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryTripod (photography)reaction center mimicryGeneral ChemistryPorphyrin0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryZincchemistryIntramolecular forceclick chemistry[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryClick chemistryQuantum TheoryFullerenesporphyrinOxidation-ReductionJournal of the American Chemical Society
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Strategies for Exploring Functions from Dynamic Combinatorial Libraries

2020

Dynamic combinatorial chemistry (DCC) is a powerful approach for creating complex chemical systems, giving access to the studies of complexity and exploration of functionality in synthetic systems. However, compared with more advanced living systems, the man‐made chemical systems are still less functional, due to their limited complexity and insufficient kinetic control. Here we start by introducing strategies to enrich the complexity of dynamic combinatorial libraries (DCLs) for exploiting unexpected functions by increasing the species of building blocks and/or templates used. Then, we discuss how dynamic isomerization of photo‐switchable molecules help DCLs increase and alter the systemic…

dynamic combinatorial chemistrynoncovalent interactionskemiallinen synteesisupramolekulaarinen kemiakinetic controlchemical complexitykompleksisuussupramolecular chemistry
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Endokrinologische Vorhersage der Therapieansprechbarkeit depressiver Patienten auf Lofepramin

1979

In a pilot study of 15 depressive patients of the neurotic and endogenous type we could show that some neuroendocrinological parameters are apt to predict the thymoleptic efficacy of lofepramine. These parameters, which were measured with a simple global stimulation test (insulin hypoglycaemia combined with injection of TRH and LHRH), were as follows: high basal blood glucose; high hypoglycaemic blood glucose; high decrease of blood glucose in comparison to the basal level; low basal TSH; low increase of HGH and low increase of cortisol after hypoglycemia. A synopsis of these parameters allowed a correct classification of 14 out of 15 patients according to therapy response and therapy resis…

endocrine systemmedicine.medical_specialtybusiness.industryStimulationEndogenyGeneral MedicineHypoglycemiamedicine.diseasePsychiatry and Mental healthInsulin hypoglycaemiaEndocrinologyBasal (medicine)Internal medicinemedicinePharmacology (medical)businesshormones hormone substitutes and hormone antagonistsBiological PsychiatryLofepramineHydrocortisonemedicine.drugEndocrine glandArchiv f�r Psychiatrie und Nervenkrankheiten
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Fluorescent naphthalimide-imidazolium hydrogels for biomedical applications

2019

Bioimaging and in vivo imaging are cornerstone technologies in support of biomedical diagnosis. However, in some cases imaging methods have increased cancer risks for patients. Moreover, the most widely used diagnostic medical imaging technique, X-ray imaging, is the largest man-made source of radiation exposure to the general population. Thus, the research of new efficient and less invasive materials for imaging is quite urgent. Supramolecular hydrogels have recently proved to be promising biological carriers to load versatile bioimaging agents for in vitro or in vivo bioimaging, thanks to the ability to undergo reversible swelling and gel–sol transition in response to various physiologica…

fluorescent hydrogels supramolecular gels imidazolium organic salts bio-imaging
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Supramolecular Association of Halochromic Switches and Halloysite Nanotubes in Fluorescent Nanoprobes for Tumor Detection

2022

Fluorescence imaging has become an indispensable tool in the biomedical laboratory to elucidate the fundamental dynamic and structural factors regulating cellular processes. The development of fluorescent nanoprobes represents a challenge to detect any cellular process under a microscope. Herein, a fluorescent nanomaterial was synthesized by exploiting the supramolecular interaction between a halochromic switch (1Cl) and halloysite nanotubes (HNTs). The successful synthesis of a HNTs/1Cl nanomaterial was confirmed by thermogravimetric analysis and Fourier transform infrared. The aqueous mobility was investigated by dynamic light scattering and ζ-potential measurements as well. Furthermore, …

fluorescent probesMCF-7 cell linesSettore BIO/14 - FarmacologiaHL-60R cell linesGeneral Materials Sciencehalloysite nanotubesSettore CHIM/06 - Chimica Organicatumor detectionhalochromic switchessupramolecular interactionsSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliSettore CHIM/02 - Chimica Fisica
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