Results 11 to 20 of about 14,652 (153)

Conformation-Dependent Electron Donation of Nido-Carborane Substituents and Its Influence on Phosphorescence of Tris(2,2′-bipyridyl)ruthenium(II) Complex

open access: yesCrystals, 2022
In this work, we report the synthesis of the nido-carborane-substituted ruthenium complexes and the substituent effects of nido-carboranes on the optical properties.
Kyoya Uemura   +2 more
doaj   +2 more sources

Synthesis of a novel planar-chiral nido-carborane amino acid [PDF]

open access: yesRussian Chemical Bulletin, 2021
The deboronation of enantiomers of planar-chiral benzyl (3-formamido-1,2-dicarba-closo-dodecaboran-1-yl)acetate gave the individual (RP)- and (SP)-enantiomers (ee > 98%) of a new amino acid containing a nido-carborane fragment, (3-ammonio-7,8-dicarba-nido-undecaboran-7-yl)acetic acid.
Telegina, A. A.   +3 more
openaire   +3 more sources

Synthesis and Reactivity of Cyclic Oxonium Derivatives of nido-Carborane: A Review

open access: yesReactions, 2022
Nucleophilic ring-opening reactions of cyclic oxonium derivatives of anionic boron hydrides are a convenient method of their modification which opens practically unlimited prospects for their incorporation into various macro- and biomolecules.
Marina Yu. Stogniy, Igor B. Sivaev
doaj   +2 more sources

Structure-Activity Relationships of <i>closo</i>- and <i>nido</i>-Carborane Erlotinib Analogs: Lipophilicity as a Key Modulator of Anti-Glioma Activity. [PDF]

open access: yesPharmaceuticals (Basel)
Background/Objectives: To enhance the anti-glioma activity of erlotinib, we previously developed a series of carborane-based analogs exploiting the concept of three-dimensional bioisosterism.
Dávila B   +8 more
europepmc   +2 more sources

Emerging agents for boron neutron capture therapy: Biomolecular carriers paving the way for precision radiotherapy. [PDF]

open access: yesPrecis Radiat Oncol
Boron neutron capture therapy (BNCT) requires key non‐negotiable technical criteria: megadose administration, precise tumor‐specific targeting, favorable biocompatibility, and sustained tumor retention. Overcoming these interconnected challenges fundamentally depends on biomolecular carriers, which are critical for translating the therapeutic potential
Chen C   +6 more
europepmc   +2 more sources

Nucleophilic Addition Reactions to 10-Acetonitrilium Derivative of nido-Carborane and Intramolecular NH⋯HB Interactions in N-Alkyl Amidines 10-RNHC(Me)=NH-7,8-C2B9H11. [PDF]

open access: yesMolecules
The addition reactions of water, alcohols, and primary and secondary amines to the 10-acetonitrilium derivative of nido-carborane were studied. Hydrolysis of 10-MeC≡N-7,8-C2B9H11 results in iminol 10-MeC(OH)=HN-7,8-C2B9H11, which, on treatment with a ...
Pakholkov KR   +6 more
europepmc   +2 more sources

Dimethyloxonium and Methoxy Derivatives of nido-Carborane and Metal Complexes Thereof

open access: yesInorganics, 2019
9-Dimethyloxonium, 10-dimethyloxonium, 9-methoxy and 10-methoxy derivatives of nido-carborane (9-Me2O-7,8-C2B9H11, 10-Me2O-7,8-C2B9H11, [9-MeO-7,8-C2B9H11]−, and [10-MeO-7,8-C2B9H11]−, respectively) were prepared by the reaction of the parent
Marina Yu. Stogniy   +4 more
doaj   +2 more sources

Synthesis and Structure of Nido-Carboranyl Azide and Its “Click” Reactions

open access: yesMolecules, 2021
Novel zwitter-ionic nido-carboranyl azide 9-N3(CH2)3Me2N-nido-7,8-C2B9H11 was prepared by the reaction of 9-Cl(CH2)3Me2N-nido-7,8-C2B9H11 with NaN3.
Anna A. Druzina   +6 more
doaj   +2 more sources

Site-Selective B─H Activation via HAT Toward Xanthyl-closo-Carboranes as Bench-Stable Precursors of Organosulfur Boron Clusters. [PDF]

open access: yesAngew Chem Int Ed Engl
A light mediated direct regioselective B─H functionalization, via hydrogen atom transfer (HAT), is described. Unexplored xanthyl‐closo‐carboranes as novel bench‐stable and versatile platforms to access sulfur‐containing boron clusters are reported for the first time.
Rusconi M   +9 more
europepmc   +3 more sources

A Redox-Tunable Carborane Crown: Toward Highly Selective Electrochemical Lithium Capture. [PDF]

open access: yesChemistry
Electrochemical reduction transforms a new carborane–crown into a potent 2e− reduced nido anion with a redox‐tunable cavity that captures Li⁺ selectively over Na⁺ and K⁺. The coupling of electronic control and size‐matched binding offers a blueprint for selective, rapid lithium recovery for next‐generation direct lithium extraction. Abstract Lithium is
Heinrich S   +6 more
europepmc   +2 more sources

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