In the polymerization of 1,3 butadiene, chain growth occurs via addition of the monomer at 1,2 or 1,4 positions; in the latter case, cis 1,4 and trans 1,4 configurations can form.It is well known [1,2] that the configurational-iso metric composition (c, t, v) along with other micro structure parameters (monomer unit distributions in a chain, average length of monomer block sequences, specific content of possible combinations of units, etc.) exert the decisive effect on the properties of PB. The relationship between the parameters (c, t, v) and properties of PB is still at the focus of researchers' attention [3][4][5][6][7]. In this case, the question arises as to whether the determination of the above parameters is correct [6].The structure of PB is investigated with the use of such nondestructive methods as vibrational spectros copy (IR and Raman) [8][9][10][11][12][13][14][15] and high resolution NMR . In research and industrial laborato ries, IR spectroscopy is the most popular method owing to its accessibility and simplicity. However, for quantitative measurements, this method requires cali bration [13] and is inferior to NMR spectroscopy in informative value. Over the past half century, the structure of PB has been intensively studied with the use of NMR spectroscopy: high resolution 1 H [16-36] and 13 C [33, 37-73] NMR spectroscopy of liquid (dissolved) samples, solid state 13 C NMR spectros copy [74][75][76], and two dimensional spectroscopy [73,[77][78][79]. Despite the considerable progress of mag netic resonance techniques, solid state and multidi mensional variants are still inferior to "classical" (i.e., liquid one dimensional) NMR for solving quantita tive problems. Therefore, our study concerns only the potential of the latter method for estimating the values of c, t, and v for polybutadiene.The use of NMR spectroscopy for the quantitative analysis of the structure of PB was discussed in [11,17,30,51,59,60]. However, this problem is still topical. First, the requirements imposed on the informative level and accuracy of the NMR method [80-82], including those for the study of polymers [83], are increasing steadily. Second, a widespread opinion about the completeness of assignment and easy analy sis of the spectra of PB as the simplest diene polymer is contrary to reality [6, 71-73, 79, 84].The goal of this study is to solve a complex of meth odological problems arising during determination of the isomeric composition of PB with the use of NMR spectroscopy.
EXPERIMENTALCommercial PBs (DOW SE BR 1202D, BUNA CB 530T, DOW SE PB 5800, SKDN and SKD L rubbers manufactured by OAO Nizhnekam skneftekhim, and SKB and SKD 2 manufactured by the Kazan and Efremov synthetic rubber plants, respectively) and laboratory samples PB 11, PB 15, PB 35, PB 38, PB 55, and PB 67 were used in this study. Laboratory samples were synthesized with the use of a lithium containing initiation system, as described in [84]. The PB samples were dissolved in chloroform d and benzene d 6 (the solution concen tration was 1 wt %) when th...