University of Hyderabad

Abstract A crystal of an organic compound is the ultimate supermolecule, and its assembly, governed by chemical and geometrical factors, from individual molecules is the perfect example of solid‐state molecular recognition. Implicit in the supramolecular description of a crystal structure is the fact that molecules in a crystal are held together by noncovalent interactions. The need for rational approaches towards solid‐state structures of fundamental and practical importance has led to the emergence of crystal engineering, which seeks to understand intermolecular interactions and recognition phenomena in the context of crystal packing. The aim of crystal engineering is to establish reliable connections between molecular and supramolecular structure on the basis of intermolecular interactions. Ideally one would like to identify substructural units in a target supermolecule that can be assembled from logically chosen precursor molecules. Indeed, crystal engineering is a new organic synthesis, and the aim of this article is to show that rather than being only nominally relevant to organic chemistry, this subject is well within the mainstream, being surprisingly similar to traditional organic synthesis in concept. The details vary because one is dealing here with intermolecular interactions rather than with covalent bonds; so this article is divided into two parts. The first is concerned with strategy, highlighting the conceptual relationship between crystal engineering and organic synthesis and introduces the term supramolecular synthon . The second part emphasizes methodology, that is, the chemical and geometrical properties of specific intermolecular interactions.

A hydrogen bond, X-H...A, is an interaction wherein a hydrogen atom is attracted to two atoms, X and A, rather than just one and so acts like a bridge between them. This attraction always increases with increasing electronegativity of X and A, and in the classical view all hydrogen bonds are highly electrostatic and sometimes even partly covalent. Gradually, the concept of a hydrogen bond became more relaxed to include weaker interactions, provided some electrostatic character remains. In the limit, these weak hydrogen bonds have considerable dispersive-repulsive character and merge into van der Waals interactions. A great variety of hydrogen bonds are observed in the solid state and the aim of this article is to highlight some features common to all these bonds and further to suggest that the term hydrogen bridge is perhaps a better descriptor for them. Such a description recognizes an interaction without borders and one that admits of much variation in its relative covalent, electrostatic, and van der Waals content.

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTThe C−H···O Hydrogen Bond: Structural Implications and Supramolecular DesignGautam R. DesirajuView Author Information School of Chemistry, University of Hyderabad, Hyderabad 500 046, India Cite this: Acc. Chem. Res. 1996, 29, 9, 441–449Publication Date (Web):September 11, 1996Publication History Received4 March 1996Published online11 September 1996Published inissue 11 September 1996https://pubs.acs.org/doi/10.1021/ar950135nhttps://doi.org/10.1021/ar950135nresearch-articleACS PublicationsCopyright © 1996 American Chemical SocietyRequest reuse permissionsArticle Views8120Altmetric-Citations1550LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Acidity,Crystal structure,Crystals,Noncovalent interactions,Supramolecular chemistry Get e-Alerts

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTRecent Advances in the Baylis−Hillman Reaction and ApplicationsDeevi Basavaiah, Anumolu Jaganmohan Rao, and Tummanapalli SatyanarayanaView Author Information School of Chemistry, University of Hyderabad, Hyderabad, 500 046 India Cite this: Chem. Rev. 2003, 103, 3, 811–892Publication Date (Web):February 27, 2003Publication History Received11 October 2002Published online27 February 2003Published inissue 1 March 2003https://pubs.acs.org/doi/10.1021/cr010043dhttps://doi.org/10.1021/cr010043dresearch-articleACS PublicationsCopyright © 2003 American Chemical SocietyRequest reuse permissionsArticle Views20389Altmetric-Citations1495LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Adducts,Aldehydes,Alkyls,Hydrocarbons,Organic compounds Get e-Alerts

Crystal engineering, the design of molecular solids, is the synthesis of functional solid-state structures from neutral or ionic building blocks, using intermolecular interactions in the design strategy. Hydrogen bonds, coordination bonds, and other less directed interactions define substructural patterns, referred to in the literature as supramolecular synthons and secondary building units. Crystal engineering has considerable overlap with supramolecular chemistry, X-ray crystallography, materials science, and solid-state chemistry and yet it is a distinct discipline in itself. The subject goes beyond the traditional divisions of organic, inorganic, and physical chemistry, and this makes for a very eclectic blend of ideas and techniques. The purpose of this Review is to highlight some current challenges in this rapidly evolving subject. Among the topics discussed are the nature of intermolecular interactions and their role in crystal design, the sometimes diverging perceptions of the geometrical and chemical models for a molecular crystal, the relationship of these models to polymorphism, knowledge-based computational prediction of crystal structures, and efforts at mapping the pathway of the crystallization reaction.

Metal-halide perovskites have rapidly emerged as one of the most promising materials of the 21st century, with many exciting properties and great potential for a broad range of applications, from photovoltaics to optoelectronics and photocatalysis. The ease with which metal-halide perovskites can be synthesized in the form of brightly luminescent colloidal nanocrystals, as well as their tunable and intriguing optical and electronic properties, has attracted researchers from different disciplines of science and technology. In the last few years, there has been a significant progress in the shape-controlled synthesis of perovskite nanocrystals and understanding of their properties and applications. In this comprehensive review, researchers having expertise in different fields (chemistry, physics, and device engineering) of metal-halide perovskite nanocrystals have joined together to provide a state of the art overview and future prospects of metal-halide perovskite nanocrystal research.

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTCrystal Engineering and Organometallic ArchitectureDario Braga, Fabrizia Grepioni, and Gautam R. DesirajuView Author Information Dipartimento di Chimica G. Ciamician, Università di Bologna, Via Selmi 2, 40126 Bologna, Italy, and School of Chemistry, University of Hyderabad, PO Central University, Hyderabad 500 046, India Cite this: Chem. Rev. 1998, 98, 4, 1375–1406Publication Date (Web):May 14, 1998Publication History Received16 June 1997Revised24 February 1998Published online14 May 1998Published inissue 1 June 1998https://pubs.acs.org/doi/10.1021/cr960091bhttps://doi.org/10.1021/cr960091bresearch-articleACS PublicationsCopyright © 1998 American Chemical SocietyRequest reuse permissionsArticle Views3720Altmetric-Citations1019LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Crystal structure,Crystals,Ligands,Metals,Noncovalent interactions Get e-Alerts

ADVERTISEMENT RETURN TO ISSUEPREVReviewNEXTMitsunobu and Related Reactions: Advances and ApplicationsK. C. Kumara Swamy*, N. N. Bhuvan Kumar, E. Balaraman, and K. V. P. Pavan KumarView Author Information School of Chemistry, University of Hyderabad, Hyderabad − 500046, A. P., India* To whom correspondence should be addressed. E-mail: [email protected] or [email protected]Cite this: Chem. Rev. 2009, 109, 6, 2551–2651Publication Date (Web):April 21, 2009Publication History Received30 July 2008Published online21 April 2009Published inissue 10 June 2009https://pubs.acs.org/doi/10.1021/cr800278zhttps://doi.org/10.1021/cr800278zreview-articleACS PublicationsCopyright © 2009 American Chemical SocietyRequest reuse permissionsArticle Views70610Altmetric-Citations977LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-AlertscloseSupporting Info (1)»Supporting Information Supporting Information SUBJECTS:Alcohols,Cyclization,Ethers,Organic compounds,Reaction products Get e-Alerts

High Resolution Image Download MS PowerPoint Slide The December 2011 release of a draft United States Food and Drug Administration (FDA) guidance concerning regulatory classification of pharmaceutical cocrystals of active pharmaceutical ingredients (APIs) addressed two matters of topical interest to the crystal engineering and pharmaceutical science communities: (1) a proposed definition of cocrystals; (2) a proposed classification of pharmaceutical cocrystals as dissociable “API-excipient” molecular complexes. The Indo–U.S. Bilateral Meeting sponsored by the Indo–U.S. Science and Technology Forum titled The Evolving Role of Solid State Chemistry in Pharmaceutical Science was held in Manesar near Delhi, India, from February 2–4, 2012. A session of the meeting was devoted to discussion of the FDA guidance draft. The debate generated strong consensus on the need to define cocrystals more broadly and to classify them like salts. It was also concluded that the diversity of API crystal forms makes it difficult to classify solid forms into three categories that are mutually exclusive. This perspective summarizes the discussion in the Indo–U.S. Bilateral Meeting and includes contributions from researchers who were not participants in the meeting.

Cytokines such as interleukin-6 induce tyrosine and serine phosphorylation of Stat3 that results in activation of Stat3-responsive genes. We provide evidence that Stat3 is present in the mitochondria of cultured cells and primary tissues, including the liver and heart. In Stat3(-/-) cells, the activities of complexes I and II of the electron transport chain (ETC) were significantly decreased. We identified Stat3 mutants that selectively restored the protein's function as a transcription factor or its functions within the ETC. In mice that do not express Stat3 in the heart, there were also selective defects in the activities of complexes I and II of the ETC. These data indicate that Stat3 is required for optimal function of the ETC, which may allow it to orchestrate responses to cellular homeostasis.

The current phase of drug development is witnessing an oncoming crisis due to the combined effects of increasing R&D costs, decreasing number of new drug molecules being launched, several blockbuster drugs falling off the patent cliff, and a high proportion of advanced drug candidates exhibiting poor aqueous solubility. The traditional approach of salt formulation to improve drug solubility is unsuccessful with molecules that lack ionizable functional groups, have sensitive moieties that are prone to decomposition/racemization, and/or are not sufficiently acidic/basic to enable salt formation. Several novel examples of pharmaceutical cocrystals from the past decade are reviewed, and the enhanced solubility profiles of cocrystals are analyzed. The peak dissolution for pharmaceutical cocrystals occurs in a short time (<30 min), and high solubility is maintained over a sufficiently long period (4–6 h) for the best cases. The enhanced solubility of drug cocrystals is similar to the supersaturation phenomenon characteristic of amorphous drugs. However, in contrast to the metastable nature of amorphous phases, cocrystals are stable owing to their crystalline nature. Yet, cocrystals can exhibit dramatic solubility advantage over the stable crystalline drug form, often comparable to amorphous pharmaceuticals. The “spring and parachute” concept for amorphous drug dissolution is adapted to explain the solubility advantage of pharmaceutical cocrystals. Thus (1) the cocrystal dissociates to amorphous or nanocrystalline drug clusters (the spring), which (2) transform via fast dissolving metastable polymorphs to the insoluble crystalline modification following the Ostwald’s Law of Stages, to give (3) high apparent solubility for cocrystals and optimal drug concentration (the parachute) in the aqueous medium.

We provide a simple explanation for X-H bond contraction and the associated blue shift and decrease of intensity in IR spectrum of the so-called improper hydrogen bonds. This explanation organizes hydrogen bonds (HBs) with a seemingly random relationship between the X-H bond length (and IR frequency and its intensity) to its interaction energy. The factors which affect the X-H bond in all X-H...Y HBs can be divided into two parts: (a) The electron affinity of X causes a net gain of electron density at the X-H bond region in the presence of Y and encourages an X-H bond contraction. (b) The well understood attractive interaction between the positive H and electron rich Y forces an X-H bond elongation. For electron rich, highly polar X-H bonds (proper HB donors) the latter almost always dominates and results in X-H bond elongation, whereas for less polar, electron poor X-H bonds (pro-improper HB donors) the effect of the former is noticeable if Y is not a very strong HB acceptor. Although both the above factors increase with increasing HB acceptor ability of Y, the shortening effect dominates over a range of Ys for suitable pro-improper X-Hs resulting in a surprising trend of decreasing X-H bond length with increasing HB acceptor ability. The observed frequency and intensity variations follow naturally. The possibility of HBs which do not show any IR frequency change in the X-H stretching mode also directly follows from this explanation.

The importance of biodiversity (below and above ground) is increasingly considered for the cleanup of the metal contaminated and polluted ecosystems. This subject is emerging as a cutting edge area of research gaining commercial significance in the contemporary field of environmental biotechnology. Several microbes, including mycorrhizal and non-mycorrhizal fungi, agricultural and vegetable crops, ornamentals, and wild metal hyperaccumulating plants are being tested both in lab and field conditions for decontaminating the metalliferous substrates in the environment. As on todate about 400 plants that hyperaccumulate metals are reported. The families dominating these members are Asteraceae, Brassicaceae, Caryophyllaceae, Cyperaceae, Cunouniaceae, Fabaceae, Flacourtiaceae, Lamiaceae, Poaceae, Violaceae, and Euphobiaceae. Brassicaceae had the largest number of taxa viz. 11 genera and 87 species. Different genera of Brassicaceae are known to accumulate metals. Ni hyperaccumulation is reported in 7 genera and 72 species and Zn in 3 genera and 20 species. Thlaspi species are known to hyperaccumulate more than one metal i.e . T. caerulescence = Cd, Ni. Pb, and Zn; T. goesingense = Ni and Zn and T. ochroleucum = Ni and Zn and T. rotundifolium = Ni, Pb and Zn. Plants that hyperaccumulate metals have tremendous potential for application in remediation of metals in the environment. Significant progress in phytoremediation has been made with metals and radionuclides. This process involves rising of plants hydroponically and transplanting them into metal-polluted waters where plants absorb and concentrate the metals in their roots and shoots. As they become saturated with the metal contaminants, roots or whole plants are harvested for disposal. Most researchers believe that plants for phytoremediation should accumulate metals only in the roots. Several aquatic species have the ability to remove heavy metals from water, viz., water hyacinth ( Eichhornia crassipes (Mart.) Solms); pennywort ( Hydrocotyle umbellata L.) and duckweed ( Lemna minor L.). The roots of Indian mustard are effective in the removal of Cd, Cr, Cu, Ni, Pb, and Zn and sunflower removes Pb, U, 137 Cs, and 90 Sr from hydroponic solutions. Aquatic plants in freshwater, marine and estuarine systems act as receptacle for several metals. Hyperaccumulators accumulate appreciable quantities of metal in their tissue regardless of the concentration of metal in the soil, as long as the metal in question is present. The phytoextraction process involves the use of plants to facilitate the removal of metal contaminants from a soil matrix. In practice, metal-accumulating plants are seeded or transplanted into metal-polluted soil and are cultivated using established agricultural practices. If metal availability in the soil is not adequate for sufficient plant uptake, chelates or acidifying agents would be applied to liberate them into the soil solution. Use of soil amendments such as synthetics (ammonium thiocyanate) and natural zeolites have yielded promising results. Synthetic cross-linked polyacrylates, hydrogels have protected plant roots from heavy metals toxicity and prevented the entry of toxic metals into roots. After sufficient plant growth and metal accumulation, the above-ground portions of the plant are harvested and removed, resulting the permanent removal of metals from the site. Soil metals should also be bioavailable, or subject to absorption by plant roots. Chemicals that are suggested for this purpose include various acidifying agents, fertilizer salts and chelating materials. The retention of metals to soil organic matter is also weaker at low pH, resulting in more available metal in the soil solution for root absorption. It is suggested that the phytoextraction process is enhanced when metal availability to plant roots is facilitated through the addition of acidifying agents to the soil. Chelates are used to enhance the phytoextraction of a number of metal contaminants including Cd, Cu, Ni, Pb, and Zn Researchers initially applied hyperaccumulators to clean metal polluted soils. Several researchers have screened fast-growing, high-biomass-accumulating plants, including agronomic crops, for their ability to tolerate and accumulate metals in their shoots. Genes responsible for metal hyperaccumulation in plant tissues have been identified and cloned. Glutathione and organic acids metabolism plays a key role in metal tolerance in plants. Glutathione is ubiquitous component cells from bacteria to plants and animals. In phytoremediation of metals in the environment, organic acids play a major role in metal tolerance. Organic acids acids form complexes with metals, a process of metal detoxification. Genetic strategies and transgenic plant and microbe production and field trials will fetch phytoremediaition field applications.The importance of biodiversity and biotechnology to remediate potentially toxic metals are discussed in this paper. Brassicaceae amenable to biotechnological improvement and phytoremediation hype are highlighted.

The normal function of poly (ADP-ribose) polymerase-1 (PARP-1) is the routine repair of DNA damage by adding poly (ADP ribose) polymers in response to a variety of cellular stresses. Recently, it has become widely appreciated that PARP-1 also participates in diverse physiological and pathological functions from cell survival to several forms of cell death and has been implicated in gene transcription, immune responses, inflammation, learning, memory, synaptic functions, angiogenesis and aging. In the CNS, PARP inhibition attenuates injury in pathologies like cerebral ischemia, trauma and excitotoxicity demonstrating a central role of PARP-1 in these pathologies. PARP-1 is also a preferred substrate for several 'suicidal' proteases and the proteolytic action of suicidal proteases (caspases, calpains, cathepsins, granzymes and matrix metalloproteinases (MMPs)) on PARP-1 produces several specific proteolytic cleavage fragments with different molecular weights. These PARP-1 signature fragments are recognized biomarkers for specific patterns of protease activity in unique cell death programs. This review focuses on specific suicidal proteases active towards PARP-1 to generate signature PARP-1 fragments that can identify key proteases and particular forms of cell death involved in pathophysiology. The roles played by some of the PARP-1 fragments and their associated binding partners in the control of different forms of cell death are also discussed.

ADVERTISEMENT RETURN TO ISSUEPREVReviewADDITION / CORRECTIONThis article has been corrected. View the notice.Recent Contributions from the Baylis−Hillman Reaction to Organic ChemistryDeevi Basavaiah*, Bhavanam Sekhara Reddy, and Satpal Singh BadsaraView Author Information School of Chemistry, University of Hyderabad, Hyderabad 500 046, India* E-mail: [email protected]Cite this: Chem. Rev. 2010, 110, 9, 5447–5674Publication Date (Web):August 24, 2010Publication History Received28 August 2009Published online24 August 2010Published inissue 8 September 2010https://pubs.acs.org/doi/10.1021/cr900291ghttps://doi.org/10.1021/cr900291greview-articleACS PublicationsCopyright © 2010 American Chemical SocietyRequest reuse permissionsArticle Views21693Altmetric-Citations805LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Adducts,Alcohols,Aldehydes,Organic compounds,Reaction products Get e-Alerts

The quest for enhancing agricultural yields due to increased pressure on food production has inevitably led to the indiscriminate use of chemical fertilizers and other agrochemicals. Biofertilizers are emerging as a suitable alternative to counteract the adverse environmental impacts exerted by synthetic agrochemicals. Biofertilizers facilitate the overall growth and yield of crops in an eco-friendly manner. They contain living or dormant microbes, which are applied to the soil or used for treating crop seeds. One of the foremost candidates in this respect is rhizobacteria. Plant growth promoting rhizobacteria (PGPR) are an important cluster of beneficial, root-colonizing bacteria thriving in the plant rhizosphere and bulk soil. They exhibit synergistic and antagonistic interactions with the soil microbiota and engage in an array of activities of ecological significance. They promote plant growth by facilitating biotic and abiotic stress tolerance and support the nutrition of host plants. Due to their active growth endorsing activities, PGPRs are considered an eco-friendly alternative to hazardous chemical fertilizers. The use of PGPRs as biofertilizers is a biological approach toward the sustainable intensification of agriculture. However, their application for increasing agricultural yields has several pros and cons. Application of potential biofertilizers that perform well in the laboratory and greenhouse conditions often fails to deliver the expected effects on plant development in field settings. Here we review the different types of PGPR-based biofertilizers, discuss the challenges faced in the widespread adoption of biofertilizers, and deliberate the prospects of using biofertilizers to promote sustainable agriculture.

There are large uncertainties looming over the status and fate of the South Asian summer monsoon, with several studies debating whether the monsoon is weakening or strengthening in a changing climate. Our analysis using multiple observed datasets demonstrates a significant weakening trend in summer rainfall during 1901–2012 over the central-east and northern regions of India, along the Ganges-Brahmaputra-Meghna basins and the Himalayan foothills, where agriculture is still largely rain-fed. Earlier studies have suggested an increase in moisture availability and land-sea thermal gradient in the tropics due to anthropogenic warming, favouring an increase in tropical rainfall. Here we show that the land-sea thermal gradient over South Asia has been decreasing, due to rapid warming in the Indian Ocean and a relatively subdued warming over the subcontinent. Using long-term observations and coupled model experiments, we provide compelling evidence that the enhanced Indian Ocean warming potentially weakens the land-sea thermal contrast, dampens the summer monsoon Hadley circulation, and thereby reduces the rainfall over parts of South Asia. The response of the South Asian summer monsoon to climate change remains uncertain. Here, the authors combine observational datasets and model simulations and show that a warming Indian Ocean and weakened land-sea thermal gradient lead to significant rainfall weakening over the central Indian subcontinent.

Acidobacteria represents an underrepresented soil bacterial phylum whose members are pervasive and copiously distributed across nearly all ecosystems. Acidobacterial sequences are abundant in soils and represent a significant fraction of soil microbial community. Being recalcitrant and difficult-to-cultivate under laboratory conditions, holistic, polyphasic approaches are required to study these refractive bacteria extensively. Acidobacteria possesses an inventory of genes involved in diverse metabolic pathways, as evidenced by their pan-genomic profiles. Because of their preponderance and ubiquity in the soil, speculations have been made regarding their dynamic roles in vital ecological processes viz., regulation of biogeochemical cycles, decomposition of biopolymers, exopolysaccharide secretion, and plant growth promotion. These bacteria are expected to have genes that might help in survival and competitive colonization in the rhizosphere, leading to the establishment of beneficial relationships with plants. Exploration of these genetic attributes and more in-depth insights into the belowground mechanics and dynamics would lead to a better understanding of the functions and ecological significance of this enigmatic phylum in the soil-plant environment. This review is an effort to provide a recent update into the diversity of genes in Acidobacteria useful for characterization, understanding ecological roles, and future biotechnological perspectives.

The existence and nature of C−H···F−C interactions in crystalline fluorobenzenes 1 − 3 and 7 − 10 are discussed. These compounds were chosen because they contain only C, H, and F atoms; this is necessary in the evaluation of the weak acceptor capabilities of the C−F group. All of these compounds are liquids at room temperature, and single crystals for X-ray diffraction were grown in situ. The analysis of the C−H···F interactions that are found in all of these crystal structures takes the form of comparisons with related C−H···O/C−H···N analogues. Fluorobenzene, 1, bears a close relationship to pyridinium fluoride, pyridine 1-oxide, and benzonitrile at the level of individual interactions, showing that the character of the structure-determining intermolecular interactions in these four crystal structures are the same. Similarly, 1,4-difluorobenzene, 3, and 1,4-benzoquinone are related, the C−H···F interactions in the former playing the same structural role as the C−H···O interactions in the latter. A comparison of 3 with the unsymmetrical 1,4-dihalogenated benzenes, 4 − 6 indicates the importance of C−H···F interactions in these structures. With an increase in the F content of the molecules, the C−H acidity also increases and the C−H···F interactions in 1,3,5-trifluorobenzene, 7, and 1,2,4,5-tetrafluorobenzene, 8, become stronger and more important. Compounds 7 and 8 are structurally very similar to 1,3,5-triazine and 1,2,4,5-tetrazine, and this similarity further strengthens the argument that C−H···F interactions resemble C−H···N interactions and provides evidence for their description as weak hydrogen bonds. 1,2,3,4-Tetrafluorobenzene, 9, is polymorphic but the role of the C−H···F interactions in the two forms is similar. A comparison of the C−H···F geometries in compounds 1 − 10 with other C-, H-, and F-containing compounds in the Cambridge Structural Database reveals that the hydrogen bond properties are more pronounced in 1 − 10 . It is concluded that only when the carbon acidity is enhanced to the levels of the compounds in the present study, is the hydrogen-bond nature of the C−H···F interaction even revealed. This study also demonstrates that the C−F group prefers to form C−H···F interactions rather than F···F contacts. The behavior of organic fluorine in crystal packing is therefore quite different from the heavier halogens.

We introduce states defined by \ensuremath{\Vert}\ensuremath{\alpha},m〉=${\mathit{a}}^{\mathrm{\ifmmode^\circ\else\textdegree\fi{}}\mathit{m}}$\ensuremath{\Vert}\ensuremath{\alpha}〉 up to a normalization constant, where \ensuremath{\Vert}\ensuremath{\alpha}〉 is a coherent state and m an integer. We study the mathematical and physical properties of such states. We demonstrate phase squeezing and the sub-Poissonian character of the fields in such states. We study in detail the quasiprobability distributions and the distribution of the field quadrature. We also show how such states can be produced in nonlinear processes in cavities.