80 research outputs found
Cooperative Carbon Dioxide Adsorption in Alcoholamine- and Alkoxyalkylamine-Functionalized Metal-Organic Frameworks.
A series of structurally diverse alcoholamine- and alkoxyalkylamine-functionalized variants of the metal-organic framework Mg2 (dobpdc) are shown to adsorb CO2 selectively via cooperative chain-forming mechanisms. Solid-state NMR spectra and optimized structures obtained from van der Waals-corrected density functional theory calculations indicate that the adsorption profiles can be attributed to the formation of carbamic acid or ammonium carbamate chains that are stabilized by hydrogen bonding interactions within the framework pores. These findings significantly expand the scope of chemical functionalities that can be utilized to design cooperative CO2 adsorbents, providing further means of optimizing these powerful materials for energy-efficient CO2 separations
Cooperative Electronic and Structural Regulation in a Bioinspired Allosteric Photoredox Catalyst
Herein, we report the first allosteric photoredox catalyst regulated via constructively coupled structural and electronic control. While often synergistically exploited in nature, these two types of control mechanisms have only been applied independently in the vast majority of allosteric enzyme mimics and receptors in the literature. By embedding a model of photosystem II in a supramolecular coordination complex that responds to chloride as an allosteric effector, we show that distance and electronic control of light harvesting can be married to maximize allosteric regulation of catalytic activity. This biomimetic system is composed of a Bodipy photoantenna, which is capable of transferring excited-state energy to a photoredox pair, wherein the excitation energy is used to generate a catalytically active charge-separated state. The structural aspect of allosteric regulation is achieved by toggling the coordination chemistry of an antenna-functionalized hemilabile ligand via partial displacement from a RhI structual node using chloride. In doing so, the distance between the antenna and the central photoredox catalyst is increased, lowering the inherent efficiency of through-space energy transfer. At the same time, coordination of chloride lowers both the charge of the Rh^I node and the reduction potential of the Rh^(II/I) couple, to the extent that electronic quenching of the antenna excited state is possible via photoinduced electron transfer from the metal center. Compared to a previously developed system that operates solely via electronic regulation, the present system demonstrates that coupling electronic and structural approaches to allosteric regulation gives rise to improved switching ratios between catalytically active and inactive states. Contributions from both structural and electronic control mechanisms are probed via nuclear magnetic resonance, X-ray diffraction, electrochemical, spectroelectrochemical, and transient absorption studies. Overall, this work establishes that intertwined electronic and structural regulatory mechanisms can be borrowed from nature to build stimuli-responsive inorganic materials with potential applications in sensing, catalysis, and photonic devices
The Chandra High Energy Transmission Grating: Design, Fabrication, Ground Calibration and Five Years in Flight
Details of the design, fabrication, ground and flight calibration of the High
Energy Transmission Grating, HETG, on the Chandra X-ray Observatory are
presented after five years of flight experience. Specifics include the theory
of phased transmission gratings as applied to the HETG, the Rowland design of
the spectrometer, details of the grating fabrication techniques, and the
results of ground testing and calibration of the HETG. For nearly six years the
HETG has operated essentially as designed, although it has presented some
subtle flight calibration effects.Comment: 34 pages (including 30 figures), accepted for publication in PAS
Motor control or graded activity exercises for chronic low back pain? A randomised controlled trial
Background: Chronic low back pain remains a major health problem in Australia and around the world. Unfortunately the majority of treatments for this condition produce small effects because not all patients respond to each treatment. It appears that only 25-50% of patients respond to exercise. The two most popular types of exercise for low back pain are graded activity and motor control exercises. At present however, there are no guidelines to help clinicians select the best treatment for a patient. As a result, time and money are wasted on treatments which ultimately fail to help the patient
Haploidentical vs. sibling, unrelated, or cord blood hematopoietic cell transplantation for acute lymphoblastic leukemia
The role of haploidentical hematopoietic cell transplantation (HCT) using posttransplant cyclophosphamide (PTCy) for acute lymphoblastic leukemia (ALL) is being defined. We performed a retrospective, multivariable analysis comparing outcomes of HCT approaches by donor for adults with ALL in remission. The primary objective was to compare overall survival (OS) among haploidentical HCTs using PTCy and HLA-matched sibling donor (MSD), 8/8 HLAmatched unrelated donor (MUD), 7 /8 HLA-MUD, or umbilical cord blood (UCB) HCT. Comparing haploidentical HCT to MSD HCT, we found that OS, leukemia-free survival (LFS), nonrelapse mortality (NRM), relapse, and acute graft-versus-host disease (aGVHD) were not different but chronic GVHD (cGVHD) was higher in MSD HCT. Compared with MUD HCT, OS, LFS, and relapse were not different, but MUD HCT had increased NRM (hazard ratio [HR], 1.42; P = .02), grade 3 to 4 aGVHD (HR, 1.59; P = .005), and cGVHD. Compared with 7/8 UD HCT, LFS and relapse were not different, but 7/8 UD HCT had worse OS (HR, 1.38; P = .01) and increased NRM (HR, 2.13; P <_ .001), grade 3 to 4 aGVHD (HR, 1.86; P = .003), and cGVHD (HR, 1.72; P <_ .001). Compared with UCB HCT, late OS, late LFS, relapse, and cGVHD were not different but UCB HCT had worse early OS (<_18 months; HR, 1.93; P < .001), worse early LFS (HR, 1.40; P = .007) and increased incidences of NRM (HR, 2.08; P < .001) and grade 3 to 4 aGVHD (HR, 1.97; P < .001). Haploidentical HCT using PTCy showed no difference in survival but less GVHD compared with traditional MSD and MUD HCT and is the preferred alternative donor HCT option for adults with ALL in complete remission
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Outcomes of haploidentical vs matched sibling transplantation for acute myeloid leukemia in first complete remission.
HLA-haploidentical hematopoietic cell transplantation (Haplo-HCT) using posttransplantation cyclophosphamide (PT-Cy) has improved donor availability. However, a matched sibling donor (MSD) is still considered the optimal donor. Using the Center for International Blood and Marrow Transplant Research database, we compared outcomes after Haplo-HCT vs MSD in patients with acute myeloid leukemia (AML) in first complete remission (CR1). Data from 1205 adult CR1 AML patients (2008-2015) were analyzed. A total of 336 patients underwent PT-Cyâbased Haplo-HCT and 869 underwent MSD using calcineurin inhibitorâbased graft-versus-host disease (GVHD) prophylaxis. The Haplo-HCT group included more reduced-intensity conditioning (65% vs 30%) and bone marrow grafts (62% vs 7%), consistent with current practice. In multivariable analysis, Haplo-HCT and MSD groups were not different with regard to overall survival (P 5 .15), leukemia-free survival (P 5 .50), nonrelapse mortality (P 5 .16), relapse (P 5 .90), or grade II-IV acute GVHD (P 5 .98). However, the Haplo-HCT group had a significantly lower rate of chronic GVHD (hazard ratio, 0.38; 95% confidence interval, 0.30-0.48; P, .001). Results of subgroup analyses by conditioning intensity and graft source suggested that the reduced incidence of chronic GVHD in Haplo-HCT is not limited to a specific graft source or conditioning intensity. Center effect and minimal residual diseaseâdonor type interaction were not predictors of outcome. Our results indicate a lower rate of chronic GVHD after PT-Cyâbased Haplo-HCT vs MSD using calcineurin inhibitorâbased GVHD prophylaxis, but similar other outcomes, in patients with AML in CR1. Haplo-HCT is a viable alternative to MSD in these patients. © 2019 American Society of Hematology. All rights reserved
Small Molecule Regulation of Self-Association and Catalytic Activity in a Supramolecular Coordination Complex
The article of record as published may be found at http://dx.doi.org/10.1021/ja500214rHerein, we report the synthesis and characterization of the first
weak-link approach (WLA) supramolecular construct that employs the small
molecule regulation of intermolecular hydrogen bonding interactions for the in situ
control of catalytic activity. A biaryl urea group, prone to self-aggregation, was
functionalized with a phosphinoalkyl thioether (P,S) hemilabile moiety and
incorporated into a homoligated Pt(II) tweezer WLA complex. This urea-containing
construct, which has been characterized by a single crystal X-ray diffraction study,
can be switched in situ from a rigid fully closed state to a flexible semiopen state via
Clâ induced changes in the coordination mode at the Pt(II) structural node. FT-IR
and 1H NMR spectroscopy studies were used to demonstrate that while extensive
urea self-association persists in the flexible semiopen complex, these interactions are
deterred in the rigid, fully closed complex because of geometric and steric restraints.
Consequently, the urea moieties in the fully closed complex are able to catalyze a
Diels-Alder reaction between cyclopentadiene and methyl vinyl ketone to generate
2-acetyl-5-norbornene. The free urea ligand and the semiopen complex show no such activity. The successful incorporation and
regulation of a hydrogen bond donating catalyst in a WLA construct open the doors to a vast and rapidly growing catalogue of
allosteric catalysts for applications in the detection and amplification of organic analytes.Funded by OASD/Research & Engineering, DoD/NSSEFF Program via the Naval Postgraduate School.United States ArmyNational Science FoundationContract/Grant W91NF-11-1-0229 (USA)Awards N00244-09-1-0012 and N00244-09-1-0071 (NPS)Grant no. CHE-1149314 (NSF
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