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1 zed and characterized by elemental analysis, multinuclear NMR spectroscopy, X-ray crystallography, an
3 ned 3D zeolite counterpart, whereas FTIR and multinuclear NMR spectroscopies demonstrate synthesis of
5 pounds were fully characterized using IR and multinuclear NMR spectroscopy, elemental analysis (EA),
6 pounds were fully characterized using IR and multinuclear NMR spectroscopy, elemental analysis, and d
7 pounds were fully characterized using IR and multinuclear NMR spectroscopy, elemental analysis, natur
9 d by X-ray diffraction, (57)Fe Mossbauer and multinuclear NMR spectroscopy, and combustion analysis.
10 erized (elemental analyses, FT-IR, Raman and multinuclear NMR spectroscopy, ESI+ mass spectrometry, c
11 crystallography, UV-visible, IR, Raman, and multinuclear NMR spectroscopies, as well as by density f
14 n fully characterized by IR spectroscopy and multinuclear NMR spectroscopy as well as by single-cryst
18 robust, permitting full characterization by multinuclear NMR spectroscopy and single-crystal X-ray d
20 or surface, have been fully characterized by multinuclear NMR ((31)P and (1)H) and electrospray ioniz
21 ), 2 = (Me-DuPHOS)(2)) were characterized by multinuclear NMR and CD spectroscopy in solution and by
22 rectangles have been fully characterized by multinuclear NMR and electrospray ionization mass spectr
25 Pentafluoroferrocene was characterized by multinuclear NMR and IR spectroscopy, by cyclovoltammetr
27 uclear dihydrido Ni complex characterized by multinuclear NMR and single-crystal X-ray diffraction an
28 The compounds have been characterized by multinuclear NMR spectroscopy and electrospray ionizatio
29 The compounds have been characterized by multinuclear NMR spectroscopy and electrospray ionizatio
30 .[H][OR] and 2.[H][NHR] are characterized by multinuclear NMR spectroscopy and X-ray crystallography,
32 ollide NHC, which was fully characterized by multinuclear NMR spectroscopy as well as single-crystal
33 produced cations were fully characterized by multinuclear NMR spectroscopy at low temperature, and th
35 mplexes of uranium and were characterized by multinuclear NMR spectroscopy, single crystal X-ray diff
36 % isolated yields and fully characterized by multinuclear NMR, 2D NMR, electrospray ionization time-o
37 l complexes have been fully characterized by multinuclear NMR, FT-IR, isotopic labeling, and, in most
38 lated and spectroscopically characterized by multinuclear NMR, IR, and UV/vis spectroscopy, crystallo
39 charged macromolecules were characterized by multinuclear NMR, mass spectrometry, and physical means.
40 tically prepared, its structure confirmed by multinuclear NMR and high resolution mass spectrometry,
44 coordinate silicon centers, as determined by multinuclear NMR spectroscopy, X-ray crystallography, an
46 ecular E...O interactions was established by multinuclear NMR spectroscopy, single crystal X-ray anal
52 nd behavior in solution have been studied by multinuclear NMR spectroscopy, which supports specific i
53 in in the Mb heme pocket has been studied by multinuclear NMR with an (15)N labeled zinc porphyrin de
54 formation of the structures is supported by multinuclear NMR, ESI FT-ICR mass spectrometry, and elem
55 erization of the supramolecular triangles by multinuclear NMR, elemental analysis, and electrospray m
58 The molecules are characterized by FTIR, multinuclear NMR, mass spectrometry, and Rutherford back
59 ies of these compounds were studied by FTIR, multinuclear NMR, mass spectrometry, Rutherford backscat
60 have been characterized using (31)P and (1)H multinuclear NMR spectroscopy and electrospray ionizatio
61 m resonances and their splitting patterns in multinuclear NMR spectra of 2H indicate that the chiral
68 all been characterized by a diverse array of multinuclear NMR spectroscopic experiments including (1)
69 Characterization involves a combination of multinuclear NMR spectroscopy, combustion analysis, DFT
70 uilding blocks were investigated by means of multinuclear NMR spectroscopy and by fast atom bombardme
72 her with these control experiments, rigorous multinuclear NMR analysis, and quantum-chemical calculat
73 ePh, 5a; Ph2, 5b) using variable temperature multinuclear NMR spectroscopy (-80 to 20 degrees C).
76 )][BPh(4)] (7) which was characterized using multinuclear NMR and high-resolution mass spectrometry.
77 The chemical structures were confirmed using multinuclear NMR spectroscopy ((1)H, (13)C, (19)F, and (
79 -ray diffraction (XRD) and in solution using multinuclear NMR methods (including DOSY, EXSY, and COSY
81 )Si = MeCl(2)Si) was fully characterized via multinuclear NMR spectroscopy and X-ray crystal structur
82 ranium complexes have been characterized via multinuclear NMR, vibrational, and electronic absorption
83 sis, all these complexes were elucidated via multinuclear NMR experiments and isotopic labelling stud
86 All three TBP cages were characterized with multinuclear NMR and electrospray ionization mass spectr
87 and building blocks were characterized with multinuclear NMR spectroscopy, electrospray ionization m
88 and building blocks were characterized with multinuclear NMR spectroscopy, electrospray ionization m
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