[Fe(NCMe)](BF) is a bifunctional catalyst for styrene aziridination by nitrene transfer and heterocycle expansion by subsequent dipolar insertion.

The solvated iron(II) salt [Fe(NCMe)](BF) (Me = methyl) is shown to be a bifunctional catalyst with respect to aziridination of styrene. The salt serves as an active catalyst for nitrene transfer from PhINTs to styrene to form 2-phenyl-N-tosylaziridine (Ph = phenyl; Ts = tosyl, -S{O}-p-CHMe). The iron(II) salt also acts as a Lewis acid in non-coordinating CHCl solution, to catalyze heterolytic CN bond cleavage of the aziridine and insertion of dipolarophiles.

Global phylogeography of ridley sea turtles ( spp.): evolution, demography, connectivity, and conservation.

Unlabelled: Globally distributed marine taxa are well suited for investigations of biogeographic impacts on genetic diversity, connectivity, and population demography. The sea turtle genus includes the wide-ranging and abundant olive ridley (), and the geographically restricted and 'Critically Endangered' Kemp's ridley (). To investigate their historical biogeography, we analyzed a large dataset of mitochondrial DNA (mtDNA) sequences from olive (n = 943) and Kemp's (n = 287) ridleys, and genotyped 15 nuclear microsatellite loci in a global sample of olive ridleys (n  285).

Seascape Genetics and the Spatial Ecology of Juvenile Green Turtles.

Understanding how ocean currents impact the distribution and connectivity of marine species, provides vital information for the effective conservation management of migratory marine animals. Here, we used a combination of molecular genetics and ocean drift simulations to investigate the spatial ecology of juvenile green turtle () developmental habitats, and assess the role of ocean currents in driving the dispersal of green turtle hatchlings. We analyzed mitochondrial (mt)DNA sequenced from 358 juvenile green turtles, and from eight developmental areas located throughout the Southwest Indian Ocean (SWIO).

Competitive Intramolecular Amination as a Clock for Iron-Catalyzed Nitrene Transfer.

Reaction of the complex [(Tp)Fe(NCMe)]BF, where Tp = hydrotris(3-phenyl,5-methyl-1-pyrazolyl)borate, with the iodonium heteroylide PhI═NTs (1.5 equiv) is proposed to result in the insertion of N-tosylnitrene into one C-H bond at the ortho ring position of a 3-pyrazole phenyl substituent; subsequent deprotonation of the nascent aniline and one-electron oxidation of iron forms TsNH (0.5 equiv) as a coproduct.

A versatile Rapture (RAD-Capture) platform for genotyping marine turtles.

Advances in high-throughput sequencing (HTS) technologies coupled with increased interdisciplinary collaboration are rapidly expanding capacity in the scope and scale of wildlife genetic studies. While existing HTS methods can be directly applied to address some evolutionary and ecological questions, certain research goals necessitate tailoring methods to specific study organisms, such as high-throughput genotyping of the same loci that are comparable over large spatial and temporal scales. These needs are particularly common for studies of highly mobile species of conservation concern like marine turtles, where life history traits, limited financial resources and other constraints require affordable, adaptable methods for HTS genotyping to meet a variety of study goals.

Environmental Warming and Feminization of One of the Largest Sea Turtle Populations in the World.

Climate change affects species and ecosystems around the globe [1]. The impacts of rising temperature are particularly pertinent in species with temperature-dependent sex determination (TSD), where the sex of an individual is determined by incubation temperature during embryonic development [2]. In sea turtles, the proportion of female hatchlings increases with the incubation temperature.

Natal foraging philopatry in eastern Pacific hawksbill turtles.

The complex processes involved with animal migration have long been a subject of biological interest, and broad-scale movement patterns of many marine turtle populations still remain unresolved. While it is widely accepted that once marine turtles reach sexual maturity they home to natal areas for nesting or reproduction, the role of philopatry to natal areas during other life stages has received less scrutiny, despite widespread evidence across the taxa. Here we report on genetic research that indicates that juvenile hawksbill turtles () in the eastern Pacific Ocean use foraging grounds in the region of their natal beaches, a pattern we term natal foraging philopatry.

Hawksbill turtle terra incognita: conservation genetics of eastern Pacific rookeries.

Prior to 2008 and the discovery of several important hawksbill turtle (Eretmochelys imbricata) nesting colonies in the EP (Eastern Pacific), the species was considered virtually absent from the region. Research since that time has yielded new insights into EP hawksbills, salient among them being the use of mangrove estuaries for nesting. These recent revelations have raised interest in the genetic characterization of hawksbills in the EP, studies of which have remained lacking to date.

Structural Characterization of Thermochromic and Spin Equilibria in Solid-State Ni(detu)4Cl2 (detu = N,N'-Diethylthiourea).

Consecutive thermochromic lattice distortional and spin crossover equilibria in solid-state Ni(detu)4Cl2 (detu = N,N'-diethylthiourea) are investigated by variable-temperature X-ray crystallography (173-333 K), DFT calculations, and differential scanning calorimetry. Thermochromism and anomalous magnetism were reported previously (S. L.

Phylogeography, Genetic Diversity, and Management Units of Hawksbill Turtles in the Indo-Pacific.

Hawksbill turtle (Eretmochelys imbricata) populations have experienced global decline because of a history of intense commercial exploitation for shell and stuffed taxidermied whole animals, and harvest for eggs and meat. Improved understanding of genetic diversity and phylogeography is needed to aid conservation. In this study, we analyzed the most geographically comprehensive sample of hawksbill turtles from the Indo-Pacific Ocean, sequencing 766 bp of the mitochondrial control region from 13 locations (plus Aldabra, n = 4) spanning over 13500 km.

Does polyandry really pay off? The effects of multiple mating and number of fathers on morphological traits and survival in clutches of nesting green turtles at Tortuguero.

Despite the long debate of whether or not multiple mating benefits the offspring, studies still show contradictory results. Multiple mating takes time and energy. Thus, if females fertilize their eggs with a single mating, why to mate more than once? We investigated and inferred paternal identity and number of sires in 12 clutches (240 hatchlings) of green turtles (Chelonia mydas) nests at Tortuguero, Costa Rica.

Religious Perspectives on Human Suffering: Implications for Medicine and Bioethics.

The prevention and relief of suffering has long been a core medical concern. But while this is a laudable goal, some question whether medicine can, or should, aim for a world without pain, sadness, anxiety, despair or uncertainty. To explore these issues, we invited experts from six of the world's major faith traditions to address the following question.

Population structure and phylogeography reveal pathways of colonization by a migratory marine reptile (Chelonia mydas) in the central and eastern Pacific.

Climate, behavior, ecology, and oceanography shape patterns of biodiversity in marine faunas in the absence of obvious geographic barriers. Marine turtles are an example of highly migratory creatures with deep evolutionary lineages and complex life histories that span both terrestrial and marine environments. Previous studies have focused on the deep isolation of evolutionary lineages (>3 mya) through vicariance; however, little attention has been given to the pathways of colonization of the eastern Pacific and the processes that have shaped diversity within the most recent evolutionary time.

Electrophilic alkylation of pseudotetrahedral nickel(II) arylthiolate complexes.

A kinetic study is reported for reactions of pseudotetrahedral nickel(II) arylthiolate complexes [(Tp(R,Me))Ni-SAr] (Tp(R,Me) = hydrotris{3-R-5-methyl-1-pyrazolyl}borate, R = Me, Ph, and Ar = C6H5, C6H4-4-Cl, C6H4-4-Me, C6H4-4-OMe, 2,4,6-Me3C6H2, 2,4,6-(i)Pr3C6H2) with organic electrophiles R'X (i.e., MeI, EtI, BzBr) in low-polarity organic solvents (toluene, THF, chloroform, dichloromethane, or 1,2-dichloroethane), yielding a pseudotetrahedral halide complex [(Tp(R,Me))Ni-X] (X = Cl, Br, I) and the corresponding organosulfide R'SAr.

Steric and electronic effects on arylthiolate coordination in the pseudotetrahedral complexes [(Tp(Ph,Me))Ni-SAr] (Tp(Ph,Me) = hydrotris{3-phenyl-5-methyl-1-pyrazolyl}borate).

Synthesis and characterization of several new pseudotetrahedral arylthiolate complexes [(Tp(Ph,Me))Ni-SAr] (Tp(Ph,Me) = hydrotris{3-phenyl-5-methyl-1-pyrazolyl}borate; Ar = Ph, 2,4,6-(i)Pr3C6H2, C6H4-4-Cl, C6H4-4-Me, C6H4-4-OMe) are reported, including X-ray crystal structures of the first two complexes. With prior results, two series of complexes are spanned, [(Tp(Ph,Me))Ni-S-2,4,6-RC6H2] (R'' = H, Me, (i)Pr) plus the xylyl analogue [(Tp(Ph,Me))Ni-S-2,6-Me2C6H3], as well as [(Tp(Ph,Me))Ni-S-C6H4-4-Y] (Y = Cl, H, Me, OMe), intended to elucidate steric and/or electronic effects on arylthiolate coordination. In contrast to [(Tp(Me,Me))Ni-SAr] analogues that adopt a sawhorse conformation, the ortho-disubstituted complexes show enhanced trigonal and Ni-S-Ar bending, reflecting the size of the 3-pyrazole substituents.

Structural and spectroscopic trends in a series of half-sandwich scorpionate complexes.

Fifteen half-sandwich scorpionate complexes [(L)M(NCMe)(3)](BF(4))(n) (L = tris(3,5-dimethylpyrazol-1-yl)methane, Tpm(Me,Me), n = 2, 1(M), M = Mn, Fe, Co, Ni; L = tris(3-phenylpyrazol-1-yl)methane, Tpm(Ph), n = 2, 2(M), M = Mn, Fe, Co, Ni; L = hydrotris(3,5-dimethylpyrazol-1-yl)borate, [Tp(Me,Me)](-), n = 1, 3(M), M = Fe, Co, Ni; L = hydrotris(3-phenyl-5-methylpyrazol-1-yl)borate, [Tp(Ph,Me)](-), n = 1, 4(M), M = Mn, Fe, Co, Ni) were prepared by addition of the tripodal ligands to solvated [M(NCMe)(x)](2+) (M = Mn, x = 4; M = Fe, Co, Ni, x = 6) precursor complexes. The product complexes were characterized by (1)H NMR (except M = Mn), UV-vis-NIR, and FTIR spectroscopy. The structures of 2(Mn), 2(Ni), 3(Fe), 3(Co), and 4(Fe) were determined by X-ray crystallography.

Aerobic and hydrolytic decomposition of pseudotetrahedral nickel phenolate complexes.

Pseudotetrahedral nickel(II) phenolate complexes Tp(R,Me)Ni-OAr (Tp(R,Me) = hydrotris(3-R-5-methylpyrazol-1-yl)borate; R = Ph {1a}, Me {1b}; OAr = O-2,6-(i)Pr(2)C(6)H(3)) were synthesized as models for nickel-substituted copper amine oxidase apoenzyme, which utilizes an N(3)O (i.e., His(3)Tyr) donor set to activate O(2) within its active site for oxidative modification of the tyrosine residue.

Solid-state spin crossover of Ni(II) in a bioinspired N3S2 ligand field.

The complex Tp(Ph,Me)NiS(2)CNMe(2) [Tp(Ph,Me) = hydrotris(3-phenyl-5-methyl-1-pyrazolyl)borate] features a bioinspired N(3)S(2) ligand set supporting a five-coordinate, trigonally distorted square-pyramidal geometry in the solid state. Spin crossover of Ni(II) was demonstrated by temperature-dependent X-ray crystallography and magnetic susceptibility measurements. The crystal lattice contains two independent molecules (i.

Steric titration of arylthiolate coordination modes at pseudotetrahedral nickel(II) centers.

Several derivatives of the pseudotetrahedral phenylthiolate complex Tp(Me,Me)Ni-SPh (1), Tp(Me,Me-) = hydrotris(3,5-dimethyl-1-pyrazolyl)borate, were prepared incorporating substituted arylthiolates, including a series of ortho-substituted ligands Tp(Me,Me)Ni-SR (R = 2,6-Me(2)C(6)H(3), 2; 2,4,6-Me(3)C(6)H(2), 3; 2,4,6- (i)Pr(3)C(6)H(2), 4; and 2,6-Ph(2)C(6)H(3), 5) and a series of para-substituted complexes (R = C(6)H(4)-4-OMe, 6; C(6)H(4)-4-Me, 7; and C(6)H(4)-4-Cl, 8). The products were characterized by (1)H NMR and UV-vis spectroscopy. Spectra of 6-8 were consistent with retention of a common structure across the para-substituted series with modest perturbation of the spectral features of 1 assisting their assignment.

Harnessing scorpionate ligand equilibria for modeling reduced nickel superoxide dismutase intermediates.

Hydrotris(3-phenyl-5-methylpyrazoyl)boratonickel(II) complexes with organoxanthate or dithiocarbamate coligands equilibrate between kappa(2)- and kappa(3)-chelation modes of the scorpionate ligand in solution, connecting N2S2 square-planar and N3S2 pyramidal ligand fields and a spin crossover. The complexes also exhibit quasi-reversible oxidations at low anodic potentials, thus modeling the structure, dynamics, and redox reactivity of the reduced NiSOD active site.

Arylthiolate coordination and reactivity at pseudotetrahedral nickel(II) centers: modulation by noncovalent interactions.

Five new pseudotetrahedral nickel(II) arylthiolate complexes Tp (R,Me)Ni-SR' [(Tp (R,Me)) (-) = 2,2,2-kappa (3)-hydridotris(3-R,5-methylpyrazolyl)borate; R = Me, R' = C 6H 5 (Ph), 2,4,6-C 6H 2(CH 3) 3 (Mes); R = Ph, R' = C 6H 5 (Ph), 2,4,6-C 6H 2(CH 3) 3 (Mes), and 2,6-C 6H 3(CH 3) 2 (Xyl)] were prepared by metathesis reactions of known chloride complexes with sodium arylthiolate salts in THF. The new products were fully characterized. The effect of increasing bulk of substituents at the proximal 3-pyrazolyl and ortho-thiolate positions represented in this series was evident in spectroscopic studies (UV-vis-NIR, (1)H NMR) of the product complexes.

Kinetic analysis of the conversion of nonheme (alkylperoxo)iron(III) species to iron(IV) complexes.

Low-spin mononuclear (alkylperoxo)iron(III) complexes decompose by peroxide O-O bond homolysis to form iron(IV) species. We examined the kinetics of previously reported homolysis reactions for (alkylperoxo)iron(III) intermediates supported by TPA (tris(2-pyridylmethyl)amine) in CH3CN solution and promoted by pyridine N-oxide, and by BPMCN (N,N-bis(2-pyridylmethyl)-N,N-dimethyl-trans-1,2-diaminocyclohexane) in its cis-beta configuration in CH3CN and CH2Cl2, as well as for the previously unreported chemistry of TPA and 5-Me3TPA intermediates in acetone. Each of these reactions forms an oxoiron(IV) complex, except for the beta-BPMCN reaction in CH2Cl2 that yields a novel (hydroxo)(alkylperoxo)iron(IV) product.

Spectroscopic and kinetic studies of the reaction of [CuI(6-PhTPA)]+ with O2.

Oxygenation of [Cu(I)(6-PhTPA)](SbF(6)) in acetone at -90 degrees C produces a short-lived Cu(III)(2)(mu-O)(2) intermediate that exhibits an oxygen-isotope-sensitive nu(Cu-O) mode at 599 cm(-1) and an overtone at 1192 cm(-1). The formation of this intermediate is very fast and is second-order in copper(I) complex, implying that two copper-containing species interact in the rate-limiting step or in pre-equilibrium steps prior to the rate determining step. The decay of this intermediate was facile even at -90 degrees C but did not afford any arene hydroxylation product.