A Chromo-Fluorogenic Synthetic Canary for CO Detection Based on a Pyrenylvinyl Ruthenium(II) Complex

The chromo-fluorogenic detection of carbon monoxide in air has been achieved using a simple, inexpensive system based on ruthenium(II). This probe shows exceptional sensitivity and selectivity in its sensing behavior in the solid state. A color response visible to the naked eye is observed at 5 ppb of CO, and a remarkably clear color change occurs from orange to yellow at the onset of toxic CO concentrations (100 ppm) in air. Even greater sensitivity (1 ppb) can be achieved through a substantial increase in turn-on emission fluorescence in the presence of carbon monoxide, both in air and in solution. No response is observed with other gases including water vapor. Immobilization of the probe on a cellulose strip allows the system to be applied in its current form in a simple optoelectronic device to give a numerical reading and/or alarm.Financial support from the Spanish Government (project MAT2012-38429-C04) and the Generalitat Valenciana (project PROMETEO/2009/016) is gratefully acknowledged. M.E.M. is grateful to the Spanish Ministerio de Ciencia e Innovacion for an FPU grant. J.D.E.T.W.-E. and A.T. acknowledge the Leverhulme Trust for a grant (RPG-2012-634).Moragues Pons, ME.; Toscani, A.; Sancenón Galarza, F.; Martínez-Máñez, R.; White, A.; Wilton-Ely, JDET. (2014). A Chromo-Fluorogenic Synthetic Canary for CO Detection Based on a Pyrenylvinyl Ruthenium(II) Complex. Journal of the American Chemical Society. 136(34):11930-11933. https://doi.org/10.1021/ja507014aS11930119331363

An optoelectronic sensing device for CO detection in air based on a binuclear rhodium complex

The design, fabrication and validation of an optoelectronic sensor implemented in an easy-to-use portable device for the selective and sensitive detection of CO in air is reported herein. The system is based on the colour changes observed in the binuclear rhodium complex of formula [Rh2[(C6H4)P(C6H5)2]2(O2CCF3)2](CF3CO2H)2(1) upon coordinating CO molecules in axial positions. Complex 1 is used supported on cellulose chromatography paper. In this support, colour changes to the naked eye are observed for CO concentrations above 50 ppm. The probe is also implemented in a simple portable optoelectronic device.The cellulose support containing probe 1 in this device is placed inside a small dark chamber, is illuminated with a tricolour LED emitting at 624, 525 and 470 nm, respectively corresponding to red (R), green (G) and blue (B) light, and reflected light is detected by a photodiode. With a transimpedance amplifier, the current generated by the photodiode is transformed into a voltage compatible with the 10-bit analogue-to-digital converter (ADC) port. Colour changes are measured as the distance d between the R, G and B data of the blank (probe without CO) and that for a certain CO concentration. Typical calibration curves are fitted using a bi-exponential equation. This system offers a typical response time of a few minutes (ca. 7 min) and a limit of detection of 11 ppm. The probe in the cellulose supports is also highly reversible.The optoelectronic device is portable (dimensions 14 × 8.5 × 3.5 cm; weighs approximately 270 g) and is powered by AA batteries. In addition, no variations in experimental parameter d upon exposure to CO2, N2, O2, Ar, water-saturated air and vapours of chloroform, hexane, ethanol, acetone, methane, toluene or formaldehyde are observed. Besides, colour changes are found for acetonitrile vapour, NO and NO2, but only at high concentrations. For validation purposes, the device was used to determine the CO present in the 4-shed accumulated smoke of two cigarette types after passing smokers lungs.We thank the Spanish Government (Project MAT2012-38429-C04-01), Generalitat Valenciana (Projects PROMETE02009/016 and ISIC/2012/005) and the UPV (Project INNOVA-04-10) for support. M.E.M thanks the Spanish Ministry of Education for a Doctoral FPU Fellowship.Moragues Pons, ME.; Montes Robles, R.; Ros-Lis, JV.; Alcañiz Fillol, M.; Ibáñez Civera, FJ.; Pardo Vicente, MT.; Martínez Mañez, R. (2014). An optoelectronic sensing device for CO detection in air based on a binuclear rhodium complex. Sensors and Actuators B: Chemical. 191:257-263. https://doi.org/10.1016/j.snb.2013.09.107S25726319

Synthesis and evaluation of fluorimetric and colorimetric chemosensors for anions based on (oligo)thienyl-thiosemicarbazones

A family of heterocyclic thiosemicarbazone dyes (3a-d) containing thienyl groups has been synthesized, characterized and their chromo-fluorogenic response in acetonitrile in the presence of selected anions studied. Acetonitrile solutions of 3a-d show absorption bands in the 338-425 nm range which are modulated by the groups attached to the thiosemicarbazone moiety. The fluoride, chloride, bromide, iodide, dihydrogen phosphate, hydrogen sulfate, nitrate, acetate and anions were used in the recognition studies. Only sensing features were observed for fluoride, cyanide, acetate and dihydrogen phosphate anions. Two different chromogenic responses were found, (i) a small shift of the absorption band due to coordination of the anions with the thiourea protons and (ii) the appearance of a new red shifted band due to deprotonation of the receptor. For the latter process changes in the color solutions from pale-yellow to orange-red were observed. Fluorescence studies showed a different emission behavior according to the number of thienyl rings in the π-conjugated bridges. Stability constants for the two processes (complex formation + deprotonation) for receptors 3a-d in the presence of fluoride and acetate anions were determined from spectrophotometric titrations using the HypSpec program. The interaction of 3d with fluoride was also studied through 1H NMR titrations. Semiempirical calculations to evaluate the hydrogen-donating ability of the receptors were also performed.Fundação para a Ciência e a Tecnologia (FCT) , Acções Integradas Luso-Espanholas/CRUP, Generalitat Valenci

Antibody Complementarity-Determining Regions (CDRs) Can Display Differential Antimicrobial, Antiviral and Antitumor Activities

Background: Complementarity-determining regions (CDRs) are immunoglobulin (Ig) hypervariable domains that determine specific antibody (Ab) binding. We have shown that synthetic CDR-related peptides and many decapeptides spanning the variable region of a recombinant yeast killer toxin-like antiidiotypic Ab are candidacidal in vitro. An alanine-substituted decapeptide from the variable region of this Ab displayed increased cytotoxicity in vitro and/or therapeutic effects in vivo against various bacteria, fungi, protozoa and viruses. the possibility that isolated CDRs, represented by short synthetic peptides, may display antimicrobial, antiviral and antitumor activities irrespective of Ab specificity for a given antigen is addressed here.Methodology/Principal Findings: CDR-based synthetic peptides of murine and human monoclonal Abs directed to: a) a protein epitope of Candida albicans cell wall stress mannoprotein; b) a synthetic peptide containing well-characterized B-cell and T-cell epitopes; c) a carbohydrate blood group A substance, showed differential inhibitory activities in vitro, ex vivo and/or in vivo against C. albicans, HIV-1 and B16F10-Nex2 melanoma cells, conceivably involving different mechanisms of action. Antitumor activities involved peptide-induced caspase-dependent apoptosis. Engineered peptides, obtained by alanine substitution of Ig CDR sequences, and used as surrogates of natural point mutations, showed further differential increased/unaltered/decreased antimicrobial, antiviral and/or antitumor activities. the inhibitory effects observed were largely independent of the specificity of the native Ab and involved chiefly germline encoded CDR1 and CDR2 of light and heavy chains.Conclusions/Significance: the high frequency of bioactive peptides based on CDRs suggests that Ig molecules are sources of an unlimited number of sequences potentially active against infectious agents and tumor cells. the easy production and low cost of small sized synthetic peptides representing Ig CDRs and the possibility of peptide engineering and chemical optimization associated to new delivery mechanisms are expected to give rise to a new generation of therapeutic agents.Department of Education, Universities and Research, Basque GovermentFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Istituto Superiore di Sanita, National Research Project on A.I.D.S.Cariparma Banking FoundationBrazilian National Research CouncilUniv Parma, Sez Microbiol, Dipartimento Patol, I-43100 Parma, ItalyUniv Basque Country, Fac Med Odontol, Dept Inmunol, Microbiol Parasitol, Bilbao, SpainUniv Basque Country, Dept Enfermeria I, Bilbao, SpainUniv Milan, Dipartimento Sci Cliniche L Sacco, Sez Malattie Infettive Immunopatol, Milan, ItalyUniv Studi Parma, Dipartimento Clin Med, Nefrol Sci Prev, Parma, ItalyUniversidade Federal de São Paulo, Departamento Microbiol, Imunol Parasitol, Unidade Oncol Expt, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biofis, São Paulo, BrazilUniversidade Federal de São Paulo, Departamento Microbiol, Imunol Parasitol, Unidade Oncol Expt, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biofis, São Paulo, BrazilDepartment of Education, Universities and Research, Basque Goverment: IT-264-07FAPESP: 06/50634-2Istituto Superiore di Sanita, National Research Project on A.I.D.S.: 50G.30Istituto Superiore di Sanita, National Research Project on A.I.D.S.: 40D.14Cariparma Banking Foundation: 2004.0190Brazilian National Research Council: research fellowshipWeb of Scienc

The USDA Barley Core Collection:Genetic Diversity, Population Structure, and Potential for Genome-Wide Association Studies

New sources of genetic diversity must be incorporated into plant breeding programs if they are to continue increasing grain yield and quality, and tolerance to abiotic and biotic stresses. Germplasm collections provide a source of genetic and phenotypic diversity, but characterization of these resources is required to increase their utility for breeding programs. We used a barley SNP iSelect platform with 7,842 SNPs to genotype 2,417 barley accessions sampled from the USDA National Small Grains Collection of 33,176 accessions. Most of the accessions in this core collection are categorized as landraces or cultivars/breeding lines and were obtained from more than 100 countries. Both STRUCTURE and principal component analysis identified five major subpopulations within the core collection, mainly differentiated by geographical origin and spike row number (an inflorescence architecture trait). Different patterns of linkage disequilibrium (LD) were found across the barley genome and many regions of high LD contained traits involved in domestication and breeding selection. The genotype data were used to define 'mini-core' sets of accessions capturing the majority of the allelic diversity present in the core collection. These 'mini-core' sets can be used for evaluating traits that are difficult or expensive to score. Genome-wide association studies (GWAS) of 'hull cover', 'spike row number', and 'heading date' demonstrate the utility of the core collection for locating genetic factors determining important phenotypes. The GWAS results were referenced to a new barley consensus map containing 5,665 SNPs. Our results demonstrate that GWAS and high-density SNP genotyping are effective tools for plant breeders interested in accessing genetic diversity in large germplasm collections

Synthesis and evaluation of thiosemicarbazones functionalized with furyl moieties as new chemosensors for anion recognition

A family of heterocyclic thiosemicarbazone dyes (3a-f and 4) containing furyl groups were synthesized in good yields, characterized and their response in acetonitrile in the presence of selected anions was studied. Acetonitrile solutions of 3a-f and 4 show absorption bands in the 335-396 nm range which are modulated by the electron donor or acceptor strength of the heterocyclic systems appended to the thiosemicarbazone moiety. Fluoride, chloride, bromide, iodide, dihydrogen phosphate, hydrogen sulphate, nitrate, acetate and cyanide anions, were used in recognition studies. From these anions, only sensing features were seen for fluoride, cyanide, acetate and dihydrogen phosphate. Two clearly different chromo-fluorogenic behaviours were observed, (i) a small shift of the absorption band due to the coordination of the anions with the thiourea protons and (ii) the appearance of a new red shifted band due to deprotonation. For the latter effect, a change in the colour solution from pale yellow to purple was observed. Fluorescence studies were also in agreement with the different effects observed in the UV/Vis titrations. In this case, hydrogen bonding interactions were visible through the enhancement of the emission band, whereas deprotonation induced the appearance of a new red-shifted emission. Logarithms of stability constants for the two processes (complex formation + deprotonation) for receptors 3a-f in the presence of fluoride and acetate anions were determined from spectrophotometric titrations using the HypSpec V1.1.18 program. Semi-empirical calculations to evaluate the hydrogen-donating ability of the receptors and a prospective electrochemical characterization of compound 3b in the presence of fluoride were also performed.Fundação para a Ciência e a Tecnologia (FCT), Acções Integradas Luso-espanholas/CRUP, Generalitat Valenciana

Imidazo-anthraquinone derivatives for the chromo-fluorogenic sensing of basic anions and trivalent metal cations

Four imidazo-anthraquinone derivatives (2a-d) functionalized with different aromatic and heteroaromatic groups were synthesized, characterized and their coordination behaviour against selected anions and cations tested. Acetonitrile solutions of probes 2a-d showed charge-transfer absorption bands in the 407-465 nm range whose positions depend on the electron donor strength of the (hetero)aromatic systems appended to the electron-acceptor anthraquinone group. The four probes were also emissive with fluorescence bands in the 533-571 nm interval. The recognition ability of 2a-d was evaluated in the presence of F-, Cl-, Br-, I-, OCN-, BzO-, ClO4-, AcO-, HSO4-, H2PO4- and CN-. Of all anions tested, only F-, AcO- and H2PO4- were able to induce the appearance of new red-shifted absorption bands in the probes that were ascribed to a deprotonation process involving the N-H moiety of the imidazole ring, especially when F- was used. Moreover addition of F-, AcO- and H2PO4- induced moderate quenching in the emission of 2a-d together with the appearance of a new red-shifted emission band. The UV-visible and emission behaviour of the four probes in the presence of Cu2+, Co2+, Mg2+, Fe3+, Ba2+, Fe2+, Ni2+, Ca2+, Zn2+, Pb2+, Cd2+, Cr3+, Al3+, K+ and Li+ was also assessed. Of all cations tested, only addition of the trivalent cations Fe3+, Cr3+ and Al3+ induced the appearance of a new blue-shifted emission in 2a-d that were ascribed to a preferential coordination of these metals with the acceptor part of the probes. Moreover trivalent cations induced an important quenching of the emission for 2a-d.Fundação para a Ciência e a Tecnologia (FCT

A Chromo-Fluorogenic Synthetic “Canary” for CO Detection Based on a Pyrenylvinyl Ruthenium(II) Complex

The chromo-fluorogenic detection of carbon monoxide in air has been achieved using a simple, inexpensive system based on ruthenium(II). This probe shows exceptional sensitivity and selectivity in its sensing behavior in the solid state. A color response visible to the naked eye is observed at 5 ppb of CO, and a remarkably clear color change occurs from orange to yellow at the onset of toxic CO concentrations (100 ppm) in air. Even greater sensitivity (1 ppb) can be achieved through a substantial increase in turn-on emission fluorescence in the presence of carbon monoxide, both in air and in solution. No response is observed with other gases including water vapor. Immobilization of the probe on a cellulose strip allows the system to be applied in its current form in a simple optoelectronic device to give a numerical reading and/or alarm.Financial support from the Spanish Government (project MAT2012-38429-C04) and the Generalitat Valenciana (project PROMETEO/2009/016) is gratefully acknowledged. M.E.M. is grateful to the Spanish Ministerio de Ciencia e Innovacion for an FPU grant. J.D.E.T.W.-E. and A.T. acknowledge the Leverhulme Trust for a grant (RPG-2012-634).Moragues Pons, ME.; Toscani, A.; Sancenón Galarza, F.; Martínez-Máñez, R.; White, A.; Wilton-Ely, JDET. (2014). A Chromo-Fluorogenic Synthetic Canary for CO Detection Based on a Pyrenylvinyl Ruthenium(II) Complex. Journal of the American Chemical Society. 136(34):11930-11933. https://doi.org/10.1021/ja507014a11930119331363