Rotation-Triggered Transmetalation on a Heterobimetallic Cu/Al N-Phosphine-Oxide-Substituted Imidazolylidene Complex

A novel strategy for the preparation of heterobimetallic N-heterocyclic carbene (NHC) complexes is demonstrated using N-phosphine-oxide-substituted imidazolylidenes (PoxIms). In these heterobimetallic Cu/Al complexes, the Cu and Al centers can be either completely separated or brought near each other via the rotation of the N-phosphinoyl group in the PoxIm ligands. Triggered by this rotation, transmetalation to exchange the Cu-OtBu and Al-C6F5 bonds occurs on in situ-generated Cu/Al PoxIm complexes, and the Cu-C6F5 and Al-OtBu bonds are formed in excellent yield. On the basis of the results of mechanistic studies, including the isolation/in situ observation of key complexes and theoretical calculations, a plausible reaction mechanism for an intramolecular transmetalation is proposed to proceed via an activation complex that includes the simultaneous coordination of the phosphinoyl oxygen atom to the Cu as well as the Al centers. Furthermore, the formation of carbon-carbon bonds between Al(C6F5)3 and allyl bromide mediated/catalyzed by Cu/Al PoxIm complexes is demonstrated. Upon the consecutive transfer of three C6F5 groups from a single molecule of Al(C6F5)3, allyl pentafluorobenzene derivatives were obtained. The present results demonstrate the role of phosphine oxide in the activation of organoaluminum reagents for the transmetalation between Cu(I) complexes bearing NHCs as well as the benefit of constructing an intramolecular system based on a heterobimetallic complex to achieve efficient transmetalation by programming the encounter of two organometallic fragments.Asada T., Hoshimoto Y., Ogoshi S.. Rotation-Triggered Transmetalation on a Heterobimetallic Cu/Al N-Phosphine-Oxide-Substituted Imidazolylidene Complex. Journal of the American Chemical Society 142, 9772 (2020); https://doi.org/10.1021/jacs.0c03252

Axial chirality around N-P bonds induced by complexation between E(C6F5)3 (E = B, Al) and an N-phosphine oxide-substituted imidazolinylidene: A key intermediate in the catalytic phosphinoylation of CO2

Complexation-induced axial chirality around an N-P bond occurs upon the predominant coordination of the N-phosphinoyl group in the N-phosphine oxide-substituted imidazolinylidene (SPoxIm) to B(C6F5)3. (Ra) and (Sa) atropisomers of (κ-O-SPoxIm)B(C6F5)3 were observed independently in the single-crystal lattice and the optimized gas-phase structure. Experimental and theoretical studies confirmed that this axial chirality arises from the restricted rotation around the N-P bond, caused by the steric repulsion between the C5-H atoms of the imidazolinylidene ring and the C6F5 rings on the B(C6F5)3 unit. Conversely, this axial chirality was not certainly observed via the complexation between SPoxIm and Al(C6F5)3. The carbene carbon atoms in (κ-O-SPoxIm)E(C6F5)3 (E = B, Al) remain sufficiently nucleophilic to react with CO2, and the phosphinoylation of CO2 with SPoxIm proceeds far more rapidly in the presence of a catalytic amount of Al(C6F5)3 than in the absence of Al(C6F5)3Asada T., Hoshimoto Y., Kawakita T., et al. Axial chirality around N-P bonds induced by complexation between E(C6F5)3 (E = B, Al) and an N-phosphine oxide-substituted imidazolinylidene: A key intermediate in the catalytic phosphinoylation of CO2. Journal of Organic Chemistry 85, 14333 (2020); https://doi.org/10.1021/acs.joc.9b03210

²H-NMR study of molecular reorientation of D₂O confined into the slit-shaped micropores of activated carbon fiber

The version of record of this article, first published in Adsorption, is available online at Publisher’s website: https://doi.org/10.1007/s10450-023-00433-8Herein, the reorientation of heavy water (D2O) molecules adsorbed in the slit-type micropores of activated carbon fibers is investigated using the 2H-nuclear magnetic resonance technique. The rotational correlation times (τ c) of D2O are evaluated from the 2H spin–lattice relaxation time (T 1). The obtained τ c values are significantly influenced by both the pore-filling ratio (ϕ) and temperature, thus suggesting that the adsorption of D2O into activated carbon fibers (ACF) effectively influences the reorientation of the D2O molecules within the ACF. The reorientational motion of D2O is examined by the extended jump model. According to this model, the nanoconfinement effect, which results from the reduction in free volume around D2O, is attributed to the transition-state excluded volume effect, whereas the effect of hydrogen bonding between the D2O and surface functional groups is attributed to the transition-state hydrogen bonding effects. Furthermore, the dependence of τ c on ϕ is explained by the chemical exchange between the pore surface adsorption sites and the central space of the pore. Thus, the dynamic behavior of adsorbed D2O molecules reveals the mechanism of D2O adsorption into the ACF micropores

Main group catalysis for H2 purification based on liquid organic hydrogen carriers

Molecular hydrogen (H2) is one of the most important energy carriers. In the midterm future, a huge amount of H2 will be produced from a variety of hydrocarbon sources through conversion and removal of contaminants such as CO and CO2. However, bypassing these purification processes is desirable, given their energy consumption and environmental impact, which ultimately increases the cost of H2. Here, we demonstrate a strategy to separate H2 from a gaseous mixture of H2/CO/CO2/CH4 that can include an excess of CO and CO2 relative to H2 and simultaneously store it in N-heterocyclic compounds that act as liquid organic hydrogen carriers (LOHCs), which can be applied to produce H2 by subsequent dehydrogenation. Our results demonstrate that LOHCs can potentially be used for H2 purification from CO- and CO2-rich crude H2 in addition to their well-established use in H2 storage.Hashimoto T., Asada T., Ogoshi S., et al. Main group catalysis for H2 purification based on liquid organic hydrogen carriers. Science Advances 8, eade0189 (2022); https://doi.org/10.1126/sciadv.ade0189

Secondary autoimmune hypothalamitis with severe memory impairment 7 years after the onset of diabetes insipidus due to lymphocytic hypophysitis: a case report

Background Autoimmune hypothalamitis is a very rare neuroendocrine disorder that causes central diabetes insipidus, headache, visual impairment, and sometimes cognitive impairment. Autoimmune hypothalamitis may occur in association with autoimmune hypophysitis, including lymphocytic hypophysitis, or in isolation. It is not known whether autoimmune hypothalamitis and autoimmune hypophysitis are consecutive diseases. Case presentation A 52-year-old woman developed autoimmune hypothalamitis 7 years after developing central diabetes insipidus due to lymphocytic hypophysitis, resulting in severe memory impairment. High-dose intravenous methylprednisolone therapy improved her cognitive function and decreased the size of the lesion. Conclusion This case presented a unique clinical course, with a long period of time between the onset of autoimmune hypopituitaritis and the development of autoimmune hypothalamitis

Strategic Utilization of Multifunctional Carbene for Direct Synthesis of Carboxylic–Phosphinic Mixed Anhydride from CO2

Direct synthesis of carboxylic–phosphinic mixed anhydrides has been achieved by treating carbon dioxide with N-phosphine oxide-substituted imidazolylidenes (PoxIms) that contain both nucleophilic carbene and electrophilic phosphorus moieties. This novel mixed anhydride was efficiently derivatized into an ester, an amide, and an unsymmetrical ketone via transformation into its corresponding imidazolium salt followed by a dual substitution reaction. The presented work used well-designed multifunctional carbene reagents to establish a novel utility for carbon dioxide in organic synthesis.Hoshimoto Y., Asada T., Hazra S., et al. Strategic Utilization of Multifunctional Carbene for Direct Synthesis of Carboxylic–Phosphinic Mixed Anhydride from CO2. Angewandte Chemie - International Edition 55, 16075 (2016); https://doi.org/10.1002/anie.201609710

Distinct effects on the secretion of MTRAP and AMA1 in Plasmodium yoelii following deletion of acylated pleckstrin homology domain-containing protein

Plasmodium, the causative agents of malaria, are obligate intracellular organisms. In humans, pathogenesis is caused by the blood stage parasite, which multiplies within erythrocytes, thus erythrocyte invasion is an essential developmental step. Merozoite form parasites released into the blood stream coordinately secrets a panel of proteins from the microneme secretory organelles for gliding motility, establishment of a tight junction with a target naive erythrocyte, and subsequent internalization. A protein identified in Toxoplasma gondii facilitates microneme fusion with the plasma membrane for exocytosis; namely, acylated pleckstrin homology domain-containing protein (APH). To obtain insight into the differential microneme discharge by malaria parasites, in this study we analyzed the consequences of APH deletion in the rodent malaria model, Plasmodium yoelii, using a DiCre-based inducible knockout method. We found that APH deletion resulted in a reduction in parasite asexual growth and erythrocyte invasion, with some parasites retaining the ability to invade and grow without APH. APH deletion impaired the secretion of microneme proteins, MTRAP and AMA1, and upon contact with erythrocytes the secretion of MTRAP, but not AMA1, was observed. APH-deleted merozoites were able to attach to and deform erythrocytes, consistent with the observed MTRAP secretion. Tight junctions were formed, but echinocytosis after merozoite internalization into erythrocytes was significantly reduced, consistent with the observed absence of AMA1 secretion. Together with our observation that APH largely colocalized with MTRAP, but less with AMA1, we propose that APH is directly involved in MTRAP secretion; whereas any role of APH in AMA1 secretion is indirect in Plasmodium

cAMP-dependent protein kinase regulates secretion of apical membrane antigen 1 (AMA1) in Plasmodium yoelii

Malaria remains a heavy global burden on human health, and it is important to understand the molecular and cellular biology of the parasite to find targets for drug and vaccine development. The mouse malaria model is an essential tool to characterize the function of identified molecules; however, robust technologies for targeted gene deletions are still poorly developed for the widely used rodent malaria parasite, Plasmodium yoelii. To overcome this problem, we established a DiCre-loxP inducible knockout (iKO) system in P. yoelii, which showed more than 80% excision efficacy of the target locus and more than 90% reduction of locus transcripts 24 h (one cell cycle) after RAP administration. Using this developed system, cAMP-dependent protein kinase (PKAc) was inducibly disrupted and the phenotypes of the resulting PKAc-iKO parasites were analyzed. We found that PKAc-iKO parasites showed severe growth and erythrocyte invasion defects. We also found that disruption of PKAc impaired the secretion of AMA1 in P. yoelii, in contrast to a report showing no role of PKAc in AMA1 secretion in P. falciparum. This discrepancy may be related to the difference in the timing of AMA1 distribution to the merozoite surface, which occurs just after egress for P. falciparum, but after several minutes for P. yoelii. Secretions of PyEBL, Py235, and RON2 were not affected by the disruption of PKAc in P. yoelii. PyRON2 was already secreted to the merozoite surface immediately after merozoite egress, which is inconsistent with the current model that RON2 is injected into the erythrocyte cytosol. Further investigations are required to understand the role of RON2 exposed on the merozoite surface

Age-specific serum anti-Müllerian hormone concentration in Japanese women and its usefulness as a predictor of the ovarian response

Purpose: To compare the ovarian response predictive ability of anti-Müllerian hormone (AMH), follicle-stimulating hormone (FSH), and estradiol (E2) and to determine the age-specific distribution of serum AMH concentrations of Japanese women. Methods: This was a multicenter (four-site), observational, analytic, cross-sectional Japanese study consisting of two parts: Study 1 (the prediction of the ovarian response of 236 participants who were undergoing controlled ovarian stimulation [COS]) and Study 2 (the distribution of the AMH concentration with an assay of 417 healthy women who were aged 20-49 years and who had normal menstrual cycles). Results: The AMH had a significantly higher predictive value for the normal and high responders than FSH and E2 as a stronger correlation between the ovarian response and AMH was observed than for FSH and E2. The serum AMH concentration decreased proportionally with age. Conclusion: The AMH concentration correlated well with the oocyte count in the patients who were undergoing COS for in vitro fertilization and was shown to predict the risk of ovarian hyperstimulation syndrome among these patients

A novel Plasmodium yoelii pseudokinase, PypPK1, is involved in erythrocyte invasion and exflagellation center formation

Malaria parasites proliferate by repeated invasion of and multiplication within erythrocytes in the vertebrate host. Sexually committed intraerythrocytic parasites undergo sexual stage differentiation to become gametocytes. After ingestion by the mosquito, male and female gametocytes egress from erythrocytes and fertilize within the mosquito midgut. A complex signaling pathway likely responds to environmental events to trigger gametogenesis and regulate fertilization; however, such knowledge remains limited for malaria parasites. Several pseudokinases are highly transcribed at the gametocyte stage and are possible multi-functional regulators controlling critical steps of the life cycle. Here we characterized one pseudokinase, termed PypPK1, in Plasmodium yoelii that is highly expressed in schizonts and male gametocytes. Immunofluorescence assays for parasites expressing Myc-tagged PypPK1 confirmed that PypPK1 protein is expressed in schizonts and sexual stage parasites. Transgenic ΔpPK1 parasites, in which the PypPK1 gene locus was deleted by the CRISPR/Cas9 method, showed significant growth defect and reduced virulence in mice. In the blood stage, ΔpPK1 parasites were able to egress from erythrocytes similar to wild type parasites; however, erythrocyte invasion efficacy was significantly reduced. During sexual stage development, no clear changes were seen in male and female gametocytemias as well as gametocyte egress from erythrocytes; but, the number of exflagellation centers and oocysts were significantly reduced in ΔpPK1 parasites. Taken together, PypPK1 has an important role for both erythrocyte invasion and exflagellation center formation