Synthesis of the first completely spin-compatible N@C60 cyclopropane derivatives by carefully tuning the DBU base catalyst

2015 ◽  
Vol 51 (33) ◽  
pp. 7096-7099 ◽  
Author(s):  
Shen Zhou ◽  
Ilija Rašović ◽  
G. Andrew D. Briggs ◽  
Kyriakos Porfyrakis
Keyword(s):  
Electron Spin ◽  
Base Catalyst ◽  
Paramagnetic Resonance ◽  
Epr Measurements ◽  
Derivatives Of ◽  
Cyclopropane Derivatives

Two cyclopropane derivatives of N@C60 were synthesised by well-controlled Bingel reactions, in which 94% of the spin centres were retained, as confirmed by a series of quantitative electron spin paramagnetic resonance (EPR) measurements.

Paramagnetic resonance and detection of a single electron spin

2001 ◽  
Vol 70 (7) ◽  
pp. 535-541 ◽  
Author(s):  
Anatolii L Buchachenko ◽  
Fedor I Dalidchik ◽  
Sergei A Kovalevskii ◽  
Boris R Shub
Keyword(s):  
Electron Spin ◽  
Single Electron ◽  
Paramagnetic Resonance

The electron spin resonance spectra and structures of some aluminium derivatives of 3,6-di-t-butyl-1,2-benzoquinone

1982 ◽  
Vol 229 (3) ◽  
pp. 215-222 ◽  
Author(s):  
Alwyn G. Davies ◽  
Zbigniew Florjańczyk ◽  
Ewa Lusztyk ◽  
Janusz Lusztyk
Keyword(s):  
Electron Spin Resonance ◽  
Electron Spin ◽  
Spin Resonance ◽  
Derivatives Of

scholarly journals Copper(II) Complexes of Organophoshonic Acids-A Comparative Study

2011 ◽  
Vol 8 (s1) ◽  
pp. S271-S281
Author(s):  
B. Venkateswara Rao ◽  
D. M. Puri
Keyword(s):  
Phosphonic Acid ◽  
Octahedral Geometry ◽  
Spectral Studies ◽  
Diphosphonic Acid ◽  
Paramagnetic Resonance ◽  
Diethylene Triamine ◽  
Coordination Sites ◽  
Infrared Spectral ◽  
Electron Paramagnetic ◽  
Derivatives Of

Polynuclear copper(II) derivatives of 1-hydroxyethylidenediphosphonic acid (HEDP), 1-aminoethylidenediphosphonic acid (AEDP, H4L),α-aminobenzylidene diphosphonic acid (ABDP, H4L), 1-amino-2-carboxyethane- 1,1-diphosphonic acid (ACEDP, H5L), 1,3 diaminopropane-1,1,3,3-tetra-phosphonic acid (DAPTP, H8L), Ethylenediamine-N,N'-bis (dimethyl-methylenephosphonic) acid (EDBDMPO, H4L),o-phenylene-diamine-N,N'-bis (dimethylmethylenephosphonic) acid (PDBDMPO, H4L), diethylene triamine –N,N,N',N',N"N-penta (methylene phosphonic) acid (DETAPMPO, H10L) and diethylene triamine –N,N"-bis (dimethyl methylene phosphonic) acid (DETBDMPO, H4L) have been prepared in aqueous medium. The general formula of derivatives from elemental analysis was found to be Cu2L.XH2O (in case of AEDP, ABDP, EDBDMPO, PDBDMPO, DETBDMPO), Cu5L2.XH2O (in case of ACEDP) Cu4L.XH2O, Cu2H4L. XH2O (in case of DAPTP) and Cu5L.XH2O (in case of DETAPMPO). The electronic spectra have shown them to be six coordinated with slight distortion from octahedral geometry. Antiferromagnetism was inferred from magnetic moment data. Infrared spectral studies were carried out to determine coordination sites. EPR (Electron Paramagnetic Resonance) spectra that supports the presence of tetragonal distortion and antiferromagnetic behaviour, have also been studied.

A Study of V3+/4+ Levels in Semi-insulating 6H-SiC using Optical Admittance and Electron Paramagnetic Resonance Spectroscopies

2006 ◽  
Vol 911 ◽  
Author(s):  
Wonwoo Lee ◽  
Mary E Zvanut
Keyword(s):  
Electron Paramagnetic Resonance ◽  
Charge State ◽  
Conduction Band ◽  
Epr Spectroscopy ◽  
Admittance Spectroscopy ◽  
Paramagnetic Resonance ◽  
Characteristic Spectrum ◽  
Epr Measurements ◽  
The Individual ◽  
Electron Paramagnetic

AbstractThe purpose of this study is to identify the vanadium acceptor levels in semi-insulating (SI) 6H-SiC using optical admittance spectroscopy (OAS) and electron paramagnetic resonance (EPR) spectroscopy. OAS conductance peaks near at 0.67 ± 0.02 eV and 0.70 ± 0.02 eV are identified as V3+/4+ levels at the quasi-cubic sites. An OAS peak at 0.87 eV is assigned to the same transition at the hexagonal site. EPR measurements before illumination revealed the characteristic spectrum of V3+. The presence of the V3+ signal supports the identification of the OAS peaks as transitions from the V3+/4+ level to the conduction band. Photo-induced EPR measurements reveal a change in the intensity of V3+ and V4+ at 0.8 ± 0.1 eV, where the amplitude of the V3+ charge state decreases and that of V4+ increases by approximately equal amounts. Although the individual sites are not resolved in the photo-induced EPR data, the 0.8 eV feature strongly supports the assignment of the three OAS peaks as acceptor levels.

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