Data are reported as follows: chemical shift, multiplicity (s = singlet, d = doublet, t = triplet, q = quartet, m = multiplet), coupling constant and integration.
Data are reported as follows: chemical shift, multiplicity (s = single, d = doublet, t = triplet, q = quartet, br = broad, and m = multiplet), integration, and coupling constants.
Data are reported as follows: chemical shift, multiplicity (s = singlet, brs = broad singlet, d = doublet, t = triplet, brt = broad triplet, q = quartet, m = multiplet), coupling constant, and integration.
Data are reported as follows: chemical shift, multiplicity (s = singlet, brs = broad singlet, d = doublet, t = triplet, brt = broad triplet, q = quartet, h = septet, m = multiplet), coupling constant, and integration.
1H NMR data are reported as follows: chemical shift, multiplicity (s = singlet, d = doublet, t = triplet, q = quartet, m = multiplet, dd = doublet of doublets, dt = doublet of triplets, td = triplet of doublets, qd = quartet of doublets), coupling constants (J) in Hertz (Hz), and integration.
Data are reported as follows: chemical shift, multiplicity (s = singlet, d = doublet, t = triplet, q = quartet, br = broad, and m = multiplet), coupling constant (Hz), and integration.
Chemical shift multiplicities are reported as s = singlet, t = triplet, q = quartet, and m = multiplet.
The 1H NMR data were represented as follows: chemical shifts, multiplicity (s. singlet, d. doublet, t. triplet, m. multiplet, br. broad) and number of protons.
Additional Data: 13C NMR Simple Survey or tabularized13C shifts, multiplicities, and intensities.
These include chemical shifts, multiplicities, peak intensity, functional groups and so on.
For 1H NMR, tetramethylsilane served as internal standard (δ = 0), and data are reported as follows: chemical shift, integration, multiplicity (s = singlet, d = doublet, t = triplet, q = quartet, m = multiplet), and coupling constant(s) in hertz.
