Four-coordinate organoboron compounds with a π-conjugated chelate ligand for optoelectronic applications

Four-coordinate organoboron compounds with a π-conjugated chelate backbone have emerged recently as highly attractive materials for a number of applications including use as emitters and electron-transport materials for organic light-emitting diodes (OLEDs) or organic field transistors, photoresponsive materials, and sensory and imaging materials. Many applications of this class of boron compounds stem from the electronic properties of the π-conjugated chelate backbone. Charge-transfer transitions from an aromatic substituent attached to the boron center of the π-conjugated chelate backbone and steric congestion have also been found to play important roles in the luminescent and photochromic properties of the four-coordinate boron compounds. This article provides an update-to-date account on the application aspects of this important class of compounds in materials science with the emphasis on OLED applications and photochromic switching.     

Organometallic chemistry related to applications for microelectronics in Japan

This is meant to be a brief overview of the developments of research activities in Japan on organometallic compounds related to their use in electronic and optoelectronic devices. The importance of organometallic compounds in the deposition of metal and semiconductor films for the fabrication of many electronic and opto-electronic devices cannot be exaggerated. Their scope has now extended to thin-film electronic ceramics and high-temperature oxide superconductors. A variety of organometallic compounds have been used as source materials in many types of processing procedures, such as metal–organic chemical vapor deposition (MOCVD), metalorganic vapor-phase epitaxy (MOVPE), metal–organic molecular-beam epitaxy (MOMBE), etc. Deposited materials include silicon, Group III–V and II–VI compound semiconductors, metals, superconducting oxides and other inorganic materials. Organometallic compounds are utilized as such in many electronic and optoelectronic devices; examples are conducting and semiconducting materials, photovoltaic, photochromic, electrochromic and nonlinear optical materials. This review consists of two parts: (I) research related to the fabrication of semiconductor, metal and inorganic materials; and (II) research related to the direct use of organometallic materials and basic fundamental research.     

Applications of Polymeric Reagents in Organic Synthesis

Summary. Polymer supported reagents have found many applications in recent years. Scientists in research laboratories of agrochemical and pharmaceutical industries now routinely utilize these compounds to prepare ensembles of small organic molecules for screening. This review is aimed to highlight some of the most important applications of these promising materials in organic synthesis. Furthermore, an extensive listing of polymeric reagents that were recently used in organic synthesis is included.     

Applications of Polymeric Reagents in Organic Synthesis

Polymer supported reagents have found many applications in recent years. Scientists in research laboratories of agrochemical and pharmaceutical industries now routinely utilize these compounds to prepare ensembles of small organic molecules for screening. This review is aimed to highlight some of the most important applications of these promising materials in organic synthesis. Furthermore, an extensive listing of polymeric reagents that were recently used in organic synthesis is included.     

Breaking Aromaticity with Aminocatalysis: A Convenient Strategy for Asymmetric Synthesis

Since the turn of the millennium, catalytic reactions promoted by primary or secondary amines have emerged as a highly useful method for organic chemistry. Very recently, the potential of such synthetic strategies has been vastly expanded by incorporating the principle of aromaticity breaking. Novel reaction pathways can now be accessed through the intermediacy of polyenamine intermediates derived from (hetero)aromatic systems. The proper design of carbonyl starting materials, combined with the high stereochemical efficiency provided by well‐established aminocatalysts, has enabled the synthesis of products with (hetero)aromatic frameworks in highly enantio‐ and diastereomerically enriched form. In this Minireview, we provide an overview of recent advances in this field of research and familiarize the reader with new synthetic opportunities offered by these interesting methodologies.     

Fluorescent “Turn‐on” Sensing Based on Metal–Organic Frameworks (MOFs)

Metal–organic frameworks (MOFs) have evolved as an exciting class of materials in the domain of porous materials. The unique features of these materials arise from the combined properties of metal ions/clusters and organic struts which form the building blocks of these fascinating architectures. Among other multifarious applications, MOFs have shown tremendous applications as sensory materials for a wide variety of species. The signal transduction induced mechanism in these confined nanospaces generate optical output in response to a particular analyte which can be detected by wide variety of detection techniques. Fluorometric methods of sensing is one of widely studied method over past few decades. MOF‐based fluorometric detection is a key research theme developed over the past few years. In this review, we give a brief overview of the recent developments of MOFs as “turn‐on” sensors for a wide range of analytes (viz. cations, anions, volatile organic compounds (VOCs), etc.).     

芴类化合物的研究新进展

芴及其衍生物是一类重要的具有刚性平面联苯结构的化合物,分子内含有较大的共轭体系,这种特殊的刚性稠环结构使芴类化合物表现出许多独特的光电性能及生物活性,在光电材料、医药等多领域具有潜在的广泛应用.更为重要的是芴类化合物易于进行结构修饰,在芴环上可方便地引入各种功能基,芴类衍生物的合成及其开拓芴类化合物潜在的新用途,成为近些年来十分活跃的研究领域,且发展迅速.结合自己的工作,参考国内外文献,全面综述了芴类化合物在有机电致发光材料、双光子吸收材料、光致变色材料、太阳能电池材料和生物医药等领域的研究与开发新进展,并对其发展趋势作了展望.     

Recent Advances in Isoindigo‐Inspired Organic Semiconductors

Over the past decade, isoindigo has become a widely used electron‐deficient subunit in donor‐acceptor organic semiconductors, and these isoindigo‐based materials have been widely used in both organic photovoltaic (OPV) devices and organic field effect transistors (OFETs). Shortly after the development of isoindigo‐based semiconductors, researchers began to modify the isoindigo structure in order to change the optoelectronic properties of the resulting materials. This led to the development of many new isoindigo‐inspired compounds; since 2012, the Kelly Research Group has synthesized a number of these isoindigo analogues and produced a variety of new donor‐acceptor semiconductors. In this Personal Account, recent progress in the field is reviewed. We describe how the field has evolved from relatively simple donor‐acceptor small molecules to structurally complex, highly planarized polymer systems. The relevance of these materials in OPV and OFET applications is highlighted, with particular emphasis on structure‐property relationships.     

金属有机框架材料对Cr(Ⅵ)离子的吸附去除研究进展

重金属离子污染问题一直备受关注.开发利用多孔材料吸附去除水中重金属离子一直是材料、环境等相关学科领域的研究热点之一.金属有机框架材料(metal-organic frameworks,MOFs)是一类新型的多孔材料,具有结构多样、比表面积大、孔径可调、孔表面特征易设计调控等特点,在气体分离、催化、传感等领域表现出极大的...     

Transition Metals in the Synthesis and Functionalization of Indoles [New Synthesis Methods (72)]

The use of transition-metal complexes as reagents for the synthesis of complex organic compounds has been under development for at least several decades, and many extraordinary organic transformations of profound potential have been realized. However, adoption of this chemistry by the practicing synthetic organic chemist has been inordinately slow, and only now are transition-metal reagents beginning to achieve their rightful place in the arsenal of organic synthesis. Several factors contributed to the initial reluctance of synthetic organic chemists to use organometallic reagents. Lacking education and experience in the ways of elements having d electrons, synthetic chemists viewed organometallic processes as something mysterious and unpredictable, and not to be discussed in polite society. Organometallic chemists did not help matters by advertising their latest advances as useful synthetic methodology, but restricting their studies to very simple organic systems lacking any serious functionality (e.g., the “methyl, ethyl, butyl, futile” syndrome). Happily, things have changed. Organometallic chemists have turned their attention to more complex systems, and more recently trained organic chemists have benefited from exposure to the application of transition metals. This combination has set the stage for major advances in the use of transition metals in the synthesis of complex organic compounds. This review deals with one aspect of this area, the use of transition metals in the synthesis of indoles.     

Organic materials with hydrostatic pressure induced mechanochromic properties

Mechanochromic organic materials are a typical class of stimuli materials that has response to external physical stimuli such as shearing, grinding, and compressing etc. Organic compounds with mechanochromic characters in solid forms have attracted significant attention in the past decades due to their potential applications in sensors and memory devices. Diamond anvil cell is an emerging technology that can provide isotropic pressure in a tiny place. Thus a new stimuli method can be applied in investigating optical variation of mechanochromic materials. In this review, we focus on mechanoluminescence systems that are responsive to isotropic compression under high pressure and summarize the recent advances on organic materials studied by the diamond anvil cell.     

Recent advances in azaborine chemistry

The chemistry of organoboron compounds has been primarily dominated by their use as powerful reagents in synthetic organic chemistry. Recently, the incorporation of boron as part of a functional target structure has emerged as a useful way to generate diversity in organic compounds. A commonly applied strategy is the replacement of a CC unit with its isoelectronic BN unit. In particular, the BN/CC isosterism of the ubiquitous arene motif has undergone a renaissance in the past decade. The parent molecule of the 1,2-dihydro-1,2-azaborine family has now been isolated. New mono- and polycyclic B,N heterocycles have been synthesized for potential use in biomedical and materials science applications. This review is a tribute to Dewar's first synthesis of a monocyclic 1,2-dihydro-1,2-azaborine 50 years ago and discusses recent advances in the synthesis and characterization of heterocycles that contain carbon, boron, and nitrogen.     

Recent synthetic applications of manganese in organic synthesis

While the organometallic compounds derived from many metals have found a broad application in organic synthesis, the use of organomanganese compounds has only recently been developed due to the passivity exhibited by commercial Mn in the direct metalation of organic compounds. In this Concept article, we highlight the potential of manganese and its organometallic compounds in organic synthesis by illustration of the studies previously reported by others and our laboratory in this field. Based on the transformations reported herein, organomanganese compounds could become important tools in the future of the organic synthesis, due to their high selectivity.     

Gold-catalyzed decorations of arenes and heteroarenes with C-C multiple bonds

Synthetic organic chemistry has been markedly affected by the booming of gold catalysis over the past decade. The renaissance of this coinage metal allowed unprecedented transformations to be realized in a highly selective manner and rendered "old chemistry" more accessible from a practical point of view. Particularly, organic compounds containing C-C multiple bonds benefited from the high carbophilicity of gold species, that opened access to a great chemical diversity through direct and selective π-electrophilic activations. Nowadays, the complexity of naturally occurring compounds based on functionalized aromatic frameworks continues to inspire and influence developments in synthetic chemistry. Furthermore, the ubiquitous presence of arene-based systems in pharmaceuticals, agrochemicals, and functional organic materials warrants the growing demand for mild, selective and sustainable synthetic routes to their preparation. In this context, although the peculiar aptitude of gold salts/complexes for interaction with aromatic compounds (auration process) has long been known, the direct catalytic gold decoration of arenes, has risen to prominence only recently. Here, the extensive use of electrophilic activation of C-C multiple bonds by gold species deserves a prominent mention, and the great strides made in the field over the last few years are described in this tutorial review.     

Synthetic Routes to Imidates and Their Applications in Organic Transformation: Recent Progress

Recent synthetic approaches and diverse applications of imidates are presented in this review. These motifs are successfully used as intermediates in organic transformations, such as the synthesis of N-heterocycles, natural products and metal complexes with a potential catalytic effect. Consequently, many attempts have been made for the development of efficient and facile synthetic methods of imidates in the past few years, as a continuum of previous paths. A wide range of organic compounds can be used as starting materials for these syntheses, including nitriles, isocyanides, amides etc. which through simple and flexible processes are converted to the desired imidates. Herein, an exploration of the recent synthetic routes of imidates and their diverse applications in organic transformations has been categorized and summarized.     

Synthesis of Anti-Inflammatory α-Arylalkanoic Acids by 1,2-Aryl Shift. New Synthetic Methods (42)

α-Arylalkanoic acids have acquired importance as anti-inflammatory agents and are now in great demand on the pharmaceutical front. Hence, the need has arisen for new and improved, economical synthetic procedures suitable for their preparation and manufacture on an industrial scale. For many years the synthetic approach to this class of compounds was restricted to the Willgerodt and Darzen reactions. More recently, several methods have been developed which are based on the 1,2-aryl shift in acetals of α-functionalized alkyl aryl ketones. This new approach starts from the oxythallation of alkyl aryl ketones first described by Taylor and McKillop in 1971. Asymmetric syntheses of some important arylakanoic acids have also been developed on this basis. The highly toxic thallium salts may be replaced, inter alia, by catalytically effective metal salts.     

Efficient Blue Electroluminescence from a Single‐layer Organic Device Composed Solely of Hydrocarbons

An interesting physical phenomenon, electroluminescence, that was originally observed with a hydrocarbon molecule has recently been developed into highly efficient organic light‐emitting devices. These modern devices have evolved through the development of multi‐element molecular materials for specific roles, and hydrocarbon devices have been left unexplored. In this study, we report an efficient organic light‐emitting device composed solely of hydrocarbon materials. The electroluminescence was achieved in the blue region by efficient fluorescence and charge recombination within a simple single‐layer architecture of macrocyclic aromatic hydrocarbons. This study may stimulate further studies on hydrocarbons to uncover their full potential as electronic materials.     

Cellulose bearing covalently linked copper phthalocyanine trisulphonate as an adsorbent selective for polycyclic compounds and its use in studies of environmental mutagens and carcinogens.

A method useful as a preconcentration technique for isolating mutagens and carcinogens is described. Cotton bearing covalently linked copper phthalocyanine trisulphonate as ligand (blue cotton) can adsorb selectively compounds having three or more fused rings. The adsorption takes place in aqueous media, involving 1:1 complex formation between the ligand and the polycyclic compound. The desorption can be done by elution with organic solvents, most effectively with methanol containing ammonia. As many important environmental mutagens and carcinogens are polycyclics, this adsorption is useful as a means of extracting this class of materials from crude samples such as food, urine and river waters. The use of copper phthalocyanine as a ligand for chromatographic supports has recently been initiated, yielding promising results for the effective separation of polycyclic aromatic compounds from each other.     

Inorganic monoliths in separation science: A review

The practical application of rigid, macro-porous organic polymer and silica based monolithic stationary phases as separation media has been described in the literature since 1992 and 1996, respectively. Today these materials are extensively used in chromatography and electrochromatography and several detailed reviews appear annually describing these materials, their synthesis and application. To compliment these publications, this review focuses upon the less commonly utilised materials for monolith synthesis, both those that have already been applied within separation science, and those that have found applications elsewhere, such as catalysis and water filtration, but have the clear potential to be explored as novel stationary phases in the near future. For the purpose of the review monoliths formed from these various alternative materials will be termed ‘Exotic Monoliths’, as these new substrates in many cases have only just begun to be explored for chromatographic separations, and in many instances have unusual and highly selective surface chemistries, which are attractive in terms of broadening the choice of monolithic materials for separation science. An extensive range of monolithic materials based on the following elements and their compounds (mostly oxides) are covered: Zr, Ti, Al, Hf, C, Au, Ag, Ce, Ge and hydroxyapatite, together with their relevant properties, methods of synthesis, and current and potential applications in separation science.     

A general, iterative, and modular approach toward carbohydrate libraries based on ruthenium-catalyzed oxidative cyclizations

Carbohydrates are an omnipresent class of highly oxygenated natural products. Due to their wide spectra of biological activities, they have been in the center of synthetic organic chemistry for more than 130 years. During the past 50 years non-natural carbohydrates attracted the interest of various chemists in the fields of organic, biological, and medical chemistry. Especially desoxygenated sugars proved to be an important class of compounds. Up to date, most non-natural analogues are synthesized starting from natural, enantiomerically pure carbohydrates in multistep synthesis. In this report, we present a synthetic strategy that allows the selective modular synthesis of natural and non-natural carbohydrates within five synthetic steps starting from readily available starting materials. Due to a sequential introduction of O- or N-functionalities, a regioselective protection of each new functional group is possible. The key step in the carbohydrate synthesis is a RuO4-catalyzed oxidative cyclization via a pH-dependent dehydrogenation-dihydroxylation-cyclization or an oxidative fragmentation-cyclization, leading to highly substituted new carbohydrates, in which each functional group is orthogonally protected and accessible for further synthetic operations.