scholarly journals EFFECTS OF COMBINED USE OF DERIVATIVES OF 4-ACETYLAMINO-NAPHTALENE-1-LAUROULSULPHONAMID AND X-RAY

1960 ◽  
Vol 10 (6) ◽  
pp. 730-747
Author(s):  
Atsuhiro Tsuchiya
Keyword(s):  
X Ray ◽  
Combined Use ◽  
Derivatives Of

Tracing young SMBHs in the dusty distant universe – a Chandra view of DOGs

2020 ◽  
Vol 15 (S359) ◽  
pp. 17-21
Author(s):  
Karín Menéndez-Delmestre ◽  
Laurie Riguccini ◽  
Ezequiel Treister
Keyword(s):  
Star Formation ◽  
Main Sequence ◽  
Far Infrared ◽  
Host Galaxy ◽  
X Ray ◽  
Star Forming ◽  
Near Ir ◽  
X Ray Imaging ◽  
Combined Use ◽  
Dusty Galaxies

AbstractThe coexistence of star formation and AGN activity has geared much attention to dusty galaxies at high redshifts, in the interest of understanding the origin of the Magorrian relation observed locally, where the mass of the stellar bulk in a galaxy appears to be tied to the mass of the underlying supermassive black hole. We exploit the combined use of far-infrared (IR) Herschel data and deep Chandra ˜160 ksec depth X-ray imaging of the COSMOS field to probe for AGN signatures in a large sample of >100 Dust-Obscured Galaxies (DOGs). Only a handful (˜20%) present individual X-ray detections pointing to the presence of significant AGN activity, while X-ray stacking analysis on the X-ray undetected DOGs points to a mix between AGN activity and star formation. Together, they are typically found on the main sequence of star-forming galaxies or below it, suggesting that they are either still undergoing significant build up of the stellar bulk or have started quenching. We find only ˜30% (6) Compton-thick AGN candidates (NH > 1024 cm–2), which is the same frequency found within other soft- and hard-X-ray selected AGN populations. This suggests that the large column densities responsible for the obscuration in Compton-thick AGNs must be nuclear and have little to do with the dust obscuration of the host galaxy. We find that DOGs identified to have an AGN share similar near-IR and mid-to-far-IR colors, independently of whether they are individually detected or not in the X-ray. The main difference between the X-ray detected and the X-ray undetected populations appears to be in their redshift distributions, with the X-ray undetected ones being typically found at larger distances. This strongly underlines the critical need for multiwavelength studies in order to obtain a more complete census of the obscured AGN population out to higher redshifts. For more details, we refer the reader to Riguccini et al. (2019).

scholarly journals Synthesis of New Derivatives of BEDT-TTF: Installation of Alkyl, Ethynyl, and Metal-Binding Side Chains and Formation of Tris(BEDT-TTF) Systems

2021 ◽  
Vol 7 (8) ◽  
pp. 110
Author(s):  
Songjie Yang ◽  
Matteo Zecchini ◽  
Andrew Brooks ◽  
Sara Krivickas ◽  
Desiree Dalligos ◽  
...  
Keyword(s):  
Metal Binding ◽  
Tricarboxylic Acid ◽  
Metal Salts ◽  
Side Chain ◽  
Side Chains ◽  
Ethynyl Group ◽  
X Ray ◽  
Transition Metal Salts ◽  
Alkyl Side Chains ◽  
Derivatives Of

The syntheses of new BEDT-TTF derivatives are described. These comprise BEDT-TTF with one ethynyl group (HC≡C-), with two (n-heptyl) or four (n-butyl) alkyl side chains, with two trans acetal (-CH(OMe)2) groups, with two trans aminomethyl (-CH2NH2) groups, and with an iminodiacetate (-CH2N(CH2CO2−)2 side chain. Three transition metal salts have been prepared from the latter donor, and their magnetic properties are reported. Three tris-donor systems are reported bearing three BEDT-TTF derivatives with ester links to a core derived from benzene-1,3,5-tricarboxylic acid. The stereochemistry and molecular structure of the donors are discussed. X-ray crystal structures of two BEDT-TTF donors are reported: one with two CH(OMe)2 groups and with one a -CH2N(CH2CO2Me)2 side chain.

The Through-Bond Interaction of a Sulfur Lone Pair with Oxygenated Substituents in the Thiacyclohexane Framework

2005 ◽  
Vol 58 (7) ◽  
pp. 531
Author(s):  
Laura Andrau ◽  
Jonathan M. White
Keyword(s):  
Low Temperature ◽  
Crystal Structures ◽  
Bond Distance ◽  
Lone Pair ◽  
X Ray ◽  
Ester Derivative ◽  
Bond Interaction ◽  
Derivatives Of ◽  
Electron Demand

Low-temperature X-ray crystal structures were determined on a range of derivatives of 4-thiacyclohexanol 5a of varying electron demand with a view to finding evidence for a through-bond interaction between the sulfur lone pair and the oxygenated substituent. In contrast to earlier suggestions, plots of C–OR bond distance versus pKa (ROH) showed that any interaction between the sulfur and the OR group is unlikely to be of a through-bond origin. Furthermore, unimolecular solvolysis rate measurements on the nosylate ester derivative 5g showed that the sulfur actually retards the reaction slightly in comparison with the corresponding sulfur-free analogue 6.

Di-n-butyltin(IV) derivatives of bis(carboxymethyl)benzylamines: synthesis, NMR and X-ray structure characterization andin vitro antitumour properties

2001 ◽  
Vol 15 (7) ◽  
pp. 593-603 ◽  
Author(s):  
Teresa Mancilla ◽  
Lourdes Carrillo ◽  
Luis S. Zamudio Rivera ◽  
Carlos Camacho Camacho ◽  
Dick de Vos ◽  
...  
Keyword(s):  
Structure Characterization ◽  
X Ray ◽  
Derivatives Of

The direct electrochemical synthesis of some metal derivatives of lapachol

1997 ◽  
Vol 75 (5) ◽  
pp. 499-506 ◽  
Author(s):  
E.H. De Oliveira ◽  
G.E.A. Medeiros ◽  
C. Peppe ◽  
Martyn A. Brown ◽  
Dennis G. Tuck
Keyword(s):  
Electrochemical Oxidation ◽  
Copper Atom ◽  
Electrochemical Synthesis ◽  
Acetonitrile Solution ◽  
Triclinic Space Group ◽  
X Ray ◽  
Metal Anode ◽  
X Ray Crystallography ◽  
Metal Derivatives ◽  
Derivatives Of

The electrochemical oxidation of a sacrificial metal anode (M = Zn, Cd, Cu) in an acetonitrile solution of 2-hydroxy-3-(3-methyl-2-butenyl)-1,4-naphthoquinone, lapachol, C15H14O3 (=HL) gives ML2. The results are in keeping with earlier work on direct electrochemical synthesis in related systems. Adducts with 2,2′-bipyridine (bpy) and N,N,N′,N′-tetramethylethanediamine (tmen) have also been prepared. The structure of the 2,2′-bipyridine adduct of Cu(lapacholate)2 has been established by X-ray crystallography. The parameters are triclinic, space group [Formula: see text], a = 12.748(59) Å, b = 13.859(49) Å, c = 11.770(59) Å, α = 108.30(4)°, β = 108.08(3)°, γ = 68.94(3)°, Z = 2, R = 0.059 for 2256 unique reflections. The copper atom is in a distorted CuN2O2O2′ environment. The mechanism of the formation of this Cu(lapacholate)2 is discussed. Keywords: electrochemical synthesis, lapachol, X-ray crystallography, copper(II) complex.

Triazene derivatives of (1,x-)diazacycloalkanes. Part VI. 3-({5,5-Dimethyl-3-[2-aryl-1-diazenyl]-1-imidazolidinyl}methyl)-4,4-dimethyl-1-[2-aryl-1-diazenyl]imidazolidines — Synthesis, characterization, and X-ray crystal structure

2006 ◽  
Vol 84 (10) ◽  
pp. 1294-1300 ◽  
Author(s):  
Keith Vaughan ◽  
Shasta Lee Moser ◽  
Reid Tingley ◽  
M Brad Peori ◽  
Valerio Bertolasi
Keyword(s):  
Crystal Structure ◽  
Significant Degree ◽  
Ion Trapping ◽  
Published Data ◽  
X Ray ◽  
X Ray Crystallography ◽  
Diazonium Ion ◽  
Derivatives Of ◽  
C Nmr

Reaction of a series of diazonium salts with a mixture of formaldehyde and 1,2-diamino-2-methylpropane affords the 3-({5,5-dimethyl-3-[2-aryl-1-diazenyl]-1-imidazolidinyl}methyl)-4,4-dimethyl-1-[2-aryl-1-diazenyl]imidazolidines (1a–1f) in excellent yield. The products have been characterized by IR and NMR spectroscopic analysis, elemental analysis, and X-ray crystallography. The X-ray crystal structure of the p-methoxycarbonyl derivative (1c) establishes without question the connectivity of these novel molecules, which can be described as linear bicyclic oligomers with two imidazolidinyl groups linked together by a one-carbon spacer. This is indeed a rare molecular building block. The molecular structure is corroborated by 1H and 13C NMR data, which correlates with the previously published data of compounds of types 5 and 6 derived from 1,3-propanediamine. The triazene moieties in the crystal of 1c display significant π conjugation, which gives the N—N bond a significant degree of double-bond character. This in turn causes restricted rotation around the N—N bond, which leads to considerable broadening of signals in both the 1H and 13C NMR spectra. The molecular ion of the p-cyanophenyl derivative (1b) was observed using electrospray mass spectrometry (ES + Na). The mechanism of formation of molecules of type 1 is proposed to involve diazonium ion trapping of the previously unreported bisimidazolidinyl methane (13).Key words: triazene, bistriazene, imidazolidine, synthesis, X-ray crystallography, NMR spectroscopy.

scholarly journals Synthesis of new half sandwich tetrachloro derivatives of molybdenum(V) and tungsten(V). X-ray structures of (C5HPri4)W(CO)3(CH3) and (C5Et5)WCl4

2002 ◽  
Vol 654 (1-2) ◽  
pp. 109-116 ◽  
Author(s):  
Matthias Bastian ◽  
Dolores Morales ◽  
Rinaldo Poli ◽  
Philippe Richard ◽  
Helmut Sitzmann
Keyword(s):  
X Ray ◽  
Derivatives Of ◽  
Half Sandwich ◽  
And Tungsten
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