Showing papers on "Carborane published in 2019"

Nonclassical Applications of closo-Carborane Anions: From Main Group Chemistry and Catalysis to Energy Storage

Abstract: Classically closo-carborane anions, particularly [HCB11H11]− and [HCB9H9]−, and their derivatives have primarily been used as weakly coordinating anions to isolate reactive intermediates, platforms for stoichiometric and catalytic functionalization, counteranions for simple Lewis acid catalysis, and components of materials like liquid crystals. The aim of this article is to educate the reader on the contemporary nonclassical applications of these anions. Specifically, this review will cover new directions in main group catalysis utilized to achieve some of the most challenging catalytic reactions such as C–F, C–H, and C–C functionalizations that are difficult or impossible to realize with transition metals. In addition, the review will cover the utilization of the clusters as dianionic C σ-bound ligands for coordination chemistry, ligand substituents for coordination chemistry and advanced catalyst design, and covalently bound spectator substituents to stabilize radicals. Furthermore, their applications a...

Controlled functionalization of o-carborane via transition metal catalyzed B–H activation

Abstract: Carboranes, a class of carbon-boron molecular clusters, are often viewed as three-dimensional analogues of benzene. They are finding increasing applications as useful functional building blocks in materials science, medicine, organometallic/coordination chemistry and more. Thus, functionalization of carboranes has received considerable attention. In comparison with the weakly acidic cage C-H bonds that can be readily functionalized, selective cage B-H functionalization among ten chemically similar BH vertices in o-carboranes is very challenging. Only in the recent few years, considerable progress has been made in transition metal catalyzed vertex-specific BH functionalization. This review summarizes recent advances in this research area.

Boron-Cluster-Enhanced Ultralong Organic Phosphorescence.

Abstract: Although carborane-based luminescent materials have been studied for years, no persistent phosphor has been reported so far. Herein, we describe boron-cluster-based persistent phosphors obtained by linking a σ-aromatic carboranyl cage to the π system of a carbazolyl group. The carboranes were found to promote intersystem crossing from a singlet to a triplet state. The rigid boron cluster was able to stabilize the ultralong triplet excitons through multiple nonclassical hydrogen bonds, such as B-H⋅⋅⋅π interactions, thus leading to a long lifetime of up to 0.666 s and an absolute phosphorescence quantum yield of 7.1 %, which is outstanding for an organic phosphor without heavy atoms. These phosphors can be excited by visible light and show dynamic emission behavior, including thermochromism and mechanochromism. This study demonstrates that non-metal/heavy-atom boron clusters can be used to develop multifunctional high-performance phosphors for potential applications.

Concept of Excitation-Driven Boron Complexes and Their Applications for Functional Luminescent Materials

Abstract: It is commonly known that flexible structures and movable substituents are unfavorable for realizing intense luminescence with organic dyes. On the other hand, we show in this short review that exc...

Multicenter‐Bond‐Based Quantum Interference in Charge Transport Through Single‐Molecule Carborane Junctions

Abstract: Molecular components are vital to introduce and manipulate quantum interference (QI) in charge transport through molecular electronic devices. Up to now, the functional molecular units that show QI are mostly found in conventional π- and σ-bond-based systems; it is thus intriguing to study QI in multicenter bonding systems without both π- and σ-conjugations. Now the presence of QI in multicenter-bond-based systems is demonstrated for the first time, through the single-molecule conductance investigation of carborane junctions. We find that all the three connectivities in carborane frameworks show different levels of destructive QI, which leads to highly suppressed single-molecule conductance in para- and meta-connected carboranes. The investigation of QI into carboranes provides a promising platform to fabricate molecular electronic devices based on multicenter bonds.

Nucleophilic substitution: a facile strategy for selective B-H functionalization of carboranes.

Abstract: Vertex-specific functionalization of carboranes has received considerable research interest, due to the valuable application of carborane derivatives in medicine, coordination/organometallic chemistry and materials. In comparison with a protic cage C-H bond, cage B-H is hydridic and generally less polar, with a bond dissociation energy of ca. 108 kcal mol-1. These features make B-H activation quite different from that of the C-H bond. In addition, selectivity among ten very similar BH vertices in o-carborane is challenging yet crucial to the effective construction of carborane-based functional molecules. To address these issues, a brand new strategy of cage B-H nucleophilic substitution has recently been presented and developed for straightforward and regioselective cage B-H functionalization. The regioselectivity can be controlled by the electronic/steric properties of the cage carbon substituents. This Frontier article highlights the recent advancement in the nucleophilic cage B-H substitution of carboranes.

Metal‐Free Oxidative B−N Coupling of nido‐Carborane with N‐Heterocycles

Abstract: A general method for the oxidative substitution of nido-carborane (7,8-C2 B9 H12 - ) with N-heterocycles has been developed by using 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) as an oxidant. This metal-free B-N coupling strategy, in both inter- and intramolecular fashions, gave rise to a wide array of charge-compensated, boron-substituted nido-carboranes in high yields (up to 97 %) with excellent functional-group tolerance under mild reaction conditions. The reaction mechanism was investigated by density-functional theory (DFT) calculations. A successive single-electron transfer (SET), B-H hydrogen-atom transfer (HAT), and nucleophilic attack pathway is proposed. This method provides a new approach to nitrogen-containing carboranes with potential applications in medicine and materials.

Synthetic Emission Tuning of Carborane-Containing Poly(dihexylfluorene)s

Abstract: Incorporation of o-carborane into the backbone of poly(dihexylfluorene)s drastically affects emission properties due to an intramolecular charge-transfer state (ICT) that forms between the fluorene...

Nitrilium derivatives of polyhedral boron compounds (boranes, carboranes, metallocarboranes): Synthesis and reactivity

Abstract: The synthesis and properties of the nitrilium derivatives of closo-dodecaborate [B12H12]2−, closo-decaborate [B10H10]2−, cobalt bis(dicarbollide) [3,3’-Co(1,2-C2B9H11)2]−, nido-decaborate [B10H14]2...

Arene-Ruthenium Complexes of 1,1'-Bis(ortho-carborane): Synthesis, Characterization, and Catalysis.

Abstract: Deprotonation of 1,1'-bis(ortho-carborane) with nBuLi in THF followed by reaction with [RuCl2(p-cymene)]2 affords, in addition to the known compound [Ru(κ3-2,2',3'-{1-(1'-closo-1',2'-C2B10H10)-closo-1,2-C2B10H10)}(p-cymene)] (I), a small amount of a new species, [Ru(κ3-2,2',11'-{1-(7'-nido-7',8'-C2B9H11)-closo-1,2-C2B10H10)}(p-cymene)] (1a), with two B-agostic B-H⇀Ru bonds, making the bis(carborane) unit a closo-nido-X(C)L2 ligand, a previously unreported bonding mode. Similar species were also formed with arene = benzene (1b), mesitylene (1c), and hexamethylbenzene (1d), although in the last two cases the metallacarborane-carborane species [1-(1'-closo-1',2'-C2B10H11)-3-(arene)-closo-3,1,2-RuC2B9H10)], 2c and 2d, were also isolated. With the bis(ortho-carborane) transfer reagent [Mg(κ2-2,2'-{1-(1'-closo-1',2'-C2B10H10)-closo-1,2-C2B10H10)}(DME)2], the target compounds [Ru(κ3-2,2',3'-{1-(1'-closo-1',2'-C2B10H10)-closo-1,2-C2B10H10)}(arene)], 4b and 4d, were prepared in reasonable-to-good yields, although for arene = benzene and mesitylene small amounts of the unique paramagnetic species [{Ru(arene)}2(μ-Cl)(μ-κ4-2,2',3,3'-{1-(1'-closo-1',2'-C2B10H9)-closo-1,2-C2B10H9})], 3b and 3c, were also formed. In compounds 3, the bis(carborane) acts as a closo-closo-X4(C,C',B,B') ligand to the Ru2 unit. In I, 4b, and 4d, the B-agostic B-H⇀Ru bond is readily cleaved by MeCN, affording compounds [Ru(κ2-2,2'-{1-(1'-closo-1',2'-C2B10H10)-closo-1,2-C2B10H10})(arene)(NCMe)] (5a, 5b, and 5d) and suggesting that I, 4b, and 4d could act as Lewis acid catalysts, which is subsequently shown to be the case for the Diels-Alder cycloaddition reactions between cyclopentadiene and methacrolein, ethylacrolein and E-crotonaldehyde. All new species were characterized by multinuclear NMR spectroscopy and 1a, 1c, 1d, 2c, 2d, 3b, 3c, 4b, 4d, 5a, 5b, and 5d were also characterized crystallographically.

Modular triazine-based carborane-containing carboxylic acids – synthesis and characterisation of potential boron neutron capture therapy agents made of readily accessible building blocks

Abstract: Based on a modular combination of s-triazine, the well-known 9-mercapto-1,7-dicarba-closo-dodecaborane(12) and commercially available carboxylic acids, namely thioglycolic acid, glycine, and Nα-Boc-l-lysine, several carboxylic acid derivatives were synthesised and fully characterised. The thioglycolic acid derivative was introduced into a peptide hormone by solid phase peptide synthesis. High activity and selective internalisation into peptide receptor-expressing cells was observed. With a very high boron content of twenty boron atoms, these derivatives are interesting as selective Boron Neutron Capture Therapy (BNCT) agents.

Metalloradicals Supported by a meta-Carborane Ligand

Abstract: In this work, a pincer-type complex [Cp*Ir-(SNPh)(SNHPh)(C2 B10 H9 )] (2) was synthesized and its reactivity studied in detail. Interestingly, molecular hydrogen can induce the transformation between the metalloradical [Cp*Ir-(SNPh)2 (C2 B10 H9 )] (5. ) and 2. A mixed-valence complex, [(Cp*Ir)2 -(SNPh)2 (C2 B10 H8 )] (7.+ ), was also synthesized by one-electron oxidation. Studies show that 7.+ is fully delocalized, possessing a four-centered-one-electron (S-Ir-Ir-S) bonding interaction. DFT calculations were also in good agreement with the experimental results.

2-Phenylpyridine- and 2-(benzo[b]thiophen-2-yl)pyridine-based o-carboranyl compounds: impact of the structural formation of aromatic rings on photophysical properties.

Abstract: 2-Phenylpyridine- and 2-(benzo[b]thiophen-2-yl)pyridine-based (ppy- and btp-based) o-carboranyl (Car1 and Car2) and their B(CH3)2-C∧N-chelated (Car1B and Car2B) compounds were prepared and fully characterised by multinuclear NMR spectroscopy and elemental analysis. The solid-state structure of Car2B was determined by single-crystal X-ray diffraction, which revealed a four-coordinated dimethylboryl centre. All compounds displayed major absorption bands that were assigned to π–π* transitions involving the ppy and btp moieties, as well as weak intramolecular charge-transfer (ICT) transitions between the o-carboranes and their aryl groups. Furthermore, the chelated compounds exhibited dominant low-energy absorption bands (λabs = 333 nm for Car1B and 383 nm for Car2B) resulting from the reinforcement of ICT transitions that correspond to the o-carborane moieties through the restriction of aromatic-ring free rotation. While Car1 and Car2 did not exhibit photoluminescence emissions in toluene at 298 K, Car1B and Car2B showed intense emissions, which are assignable to π–π* transitions associated with each chelated aryl group. However, Car1 and Car2 evidently emitted at around 450 nm in solution at 77 K, invoked by radiative ICT transitions between the carborane and the ppy or btp moiety, indicating that ICT-based radiative decay is only invigorated in the rigid state in the absence of structural variations, such as C–C bond fluctuations in the carborane cage and aromatic-ring free rotation. Interestingly, while Car1 in the film state exhibited a weak ICT-based emission spectrum, and Car1B and Car2B showed intense emissions originating from π–π* transitions associated with each chelated aryl group, Car2 showed significantly enhanced emissions in the same energy region as that exhibited in solution at 77 K, resulting in a much larger quantum efficiency over that in solution. DFT-optimised structures of Car1 and Car2 in their ground and the first-excited states clearly reveal that the enhanced emissive features of Car2 in the film state are strongly associated with the retained planarity of the btp moiety in both the ground and excited states. The photophysical results for these o-carboranyl compounds definitively reveal that the planarities of the aryl groups appended to the o-carborane decisively affect the efficiency of radiative decay based on ICT involving the o-carborane.

Simple and scalable synthesis of the carborane anion CB11H12.

Abstract: We report a method to obtain carba-closo-dodecaborate anion CB11H12- from boron cluster B11H14- in up to 95% yield using difluorocarbene to complete the carborane cluster. Difluorocarbene itself comes from readily available Ruppert-Prakash reagent CF3SiMe3. The synthesis is straightforward to carry out in heavy wall glass pressure tubes without the need for a glove-box and is easily scalable to 15 g scale.

A Phthalocyanine-ortho-Carborane Conjugate for Boron Neutron Capture Therapy: Synthesis, Physicochemical Properties, and in vitro Tests

Abstract: Boronated molecular systems can be applied to boron neutron capture therapy (BNCT). Among these systems, carborane-containing phthalocyanines (Pcs) are the most promising BNCT agents. Herein we report the new zinc (II) complex of the hexacationic Pc 6, which has been obtained as iodide salt through quaternization of the neutral precursor with methyl iodide. Compound 6 was synthesized over a sequence of four steps. The complex, and its precursors as well, were characterized by a combination of spectroscopic techniques, and their structures assessed by 1 H, 13 C, 11 B, and two-dimensional NMR spectroscopy experiments. Together with a marked tendency to aggregate, 6 showed appreciable solubility in water. Singlet oxygen quantum yield (ΦΔ ) of 0.38, and fluorescence quantum yield (ΦF ) of 0.13 were obtained for 6 in a DMF solution. The complex proved to be very effective in enriching UMR-106 cells with 10 B, showing very good performance even in case of very low concentrations exposure, i. e. 1 ppm, that moreover resulted in a mild cytotoxic effect. Such a feature can be related to the polycationic nature of the complex, and hence to the well-known propensity of positively charged species to enter the cellular membrane or to adhere to its external surface.

Recent Progress in the Synthesis of the Monocarba‐closo‐dodecaborate(−) Anions

Abstract: This Concept article focuses on the rapid growth in studies of the chemistry of the monocarba-closo-dodecaborate(-) anion (C1 carborane anion). As one of the most stable anions known, the C1 carborane anion has been useful for exploring the chemistry of highly reactive cations. On the other hand, development of novel functional molecules utilizing the unique properties of C1 carborane anion (e.g., σ-aromaticity, rigid spherical skeleton) has progressed more slowly. The main reason for this is the relatively undeveloped state of synthetic chemistry in this area. Recent advances in the synthetic chemistry of C1 carborane anion are highlighted in this Concept article, focusing on cross-coupling reactions at the carbon vertex, direct conversion of B-H bonds, and the synthesis of multivalent weakly coordinating anions. These progressions move this species beyond its well-established role of highly stable "counter" monocharged anion.

Aggregation-Induced Fluorescence of Carbazole and o -Carborane Based Organic Fluorophore.

Abstract: Carbazole based fluorophores 9-butyl-3,6-bis-(phenylethynyl)-9H-carbazole (1) and 9-butyl-3,6-bis-(2-phenyl-o-carborane)-9H-carbazole (2) were synthesized via Sonogashira type cross-coupling reaction and followed by insertion with decaborane. Compound 1 exhibited far more intense fluorescence than 2 in THF solution, while in solid state 2 exerted stronger fluorescence than 1. The fluorescence quenching behavior of 2 in THF solution could be attributed to the intramolecular charge transfer of donor-acceptor system in 2, which was confirmed by electrochemical experiments and DFT calculations. The fluorescence enhancement of 2 in solid state can be ascribed to aggregational induced packing which was evidenced by crystallographic study. In addition, compound 2 showed typical aggregation induced emission (AIE) behavior.