All manipulations were performed under nitrogen gas using standard Schlenk techniques. Research grade ethylene and propylene were purified by passing it through a deoxygenation and a dry columns. Methylene chloride and o-dichlorobenzene were pre-dried with 4 Å molecular sieves and distilled from CaH2 under dry nitrogen. Toluene, hexane, diethyl ether and 1,2-dimethoxyethane (DME) were distilled from sodium/benzophenone under nitrogen atmosphere and distilled before use. MMAO were donated by Tosoh-Finechem. Complex Ni' [25] was prepared according to reported procedures. Other chemicals were commercially obtained and purified with common procedures.

¹H and ¹³C NMR spectra were recorded with a Bruker Ascend 400 spectrometer at ambient temperature unless otherwise stated. The chemical shifts of the ¹H and ¹³C NMR spectra were referenced to tetramethylsilane (TMS). Elemental analysis was performed by the Analytical Center of the Changzhou University. X-ray diffraction data were collected at 298(2) K on a Bruker Smart CCD area detector with graphite-monochromated MoK_α radiation (λ = 0.71073 Å). Gel permeation chromatography (GPC) was carried out at 150˚C by using a PL-GPC 220 high-temperature gel permeation chromatography system. 1,2,4-Trichlorobenzene (TCB) was used as the solvent at a flow rate of 1.0 mL min^–1, and the system was calibrated by using a polystyrene standard and are corrected for linear polyethylene by universal calibration by using the Mark–Houwink parameters of Rudin: K = 1.75 × 10^–2 cm³ g^–1 and R = 0.67 for polystyrene and K = 5.90 × 10^–2 cm³ g^–1 and R = 0.69 for polyethylene.

Synthesis of (2,4-dibenzhydryl-6-phenylphenylimino)-butanone L'

A solution of 2,6-bis(diphenylmethyl)-4-phenylaniline (20 mmol) [26] , 2,3-butadione (100 mmol) and Formic acid (1mL) in methyl alcohol (80 mL) was stirred at 60˚C for 12 h, until there was one main point on the TLC plate. The solvent was partially evaporated under reduced pressure until the formation of a light yellow solid (9.10 g, 80%). ¹H NMR (400 MHz, CDCl₃, ppm): δ 7.24 - 6.98 (m, 24H), 6.94 - 6.86 (m, 2H), 6.73 (t, J = 7.6 Hz, 1H), 5.45 (d, 2H, -CHPh₂), 2.43 (s, 3H, -CH₃), 0.72 (s, 3H, -CH₃).

Synthesis of [N-(2,4-dibenzhydryl-6-phenylphenyl)-N'-(2,6-dimethylphenyl)]-2,3 -butadiene L

A mixture of L1' (5.69 g, 10 mmol), aniline (1.86 g, 10 mmol), and a catalytic amount of p-toluenesulfonic acid in 150 mL toluene was refluxed for 24 h. The solution was evaporated at reduced pressure, and the remaining solution was diluted in methanol (300 mL). The yellow solid was isolated by filtration, followed by recrystallization from dichloromethane and methanol (5.50g, 95%). ¹H NMR (400 MHz, CDCl₃, ppm): δ 7.27 (t, J = 7.6 Hz, 4H), 7.24 - 7.04 (m, 20H), 7.02 - 6.96 (m, 4H), 6.87 (t, J = 7.6 Hz, 1H), 6.74 (t, J = 7.6 Hz, 1H), 5.56 (s, 2H, -CHPh₂), 5.48 (s, 2H, -CHPh₂), 1.92 (s, 6H, -CH₃), 1.70 (s, 3H, -CH₃), 0.93 (s, 3H, -CH₃). ¹³C NMR (100 MHz, CDCl₃, ppm): δ 168.77 (C=N), 167.34 (C=N), 130.09, 129.71, 129.56, 129.37, 128.38, 128.15, 127.98, 127.75, 126.55, 126.23, 124.53, 123.12, 56.54 (-CHPh₂), 52.83 (-CHPh₂), 17.91 (-CH₃), 17.53 (-CH₃), 16.19 (-CH₃), 15.75 (-CH₃). Anal. Calcd. for C₅₀H₄₄N₂ (672.92): C, 89.25; H, 6.59; N, 4.16. Found: C, 89.29; H, 6.63; N, 4.10. FT-IR (KBr): 1649 cm⁻¹ (v_C＝N).

Synthesis of {[N-(2,4-dibenzhydryl-6-phenylphenyl)-N'-(2,6-dimethylphenyl)]-2,3-butadiene}dibromonickel Ni

A mixture of the ligand L (1 mmol), (DME)NiBr₂ (308 mg, 1 mmol) in CH₂Cl₂ (20 mL) was stirred for 2 hours at room temperature, Then concentrate the solvent, add ether to precipitate the solid catalyst, filter and clear with ether for three to five times, and vacuum dry the solid to obtain the catalyst Ni (93%, 5.50 g). Anal. Calcd. for C₅₀H₄₄Br₂N₂Ni (891.42): C, 67.37; H, 4.98; N, 3.14. Found: C, 67.41; H, 4.93; N, 3.17. FT-IR (KBr): 1643 cm⁻¹ (v_C=N).

Single crystal of ligand for X-ray analysis were obtained by dissolving the nickel complex in CH₂Cl₂, followed by slow layering of the resulting solution with at room temperature. Data collections were performed at 150 K on a Bruker SMART APEX diffractometer with a CCD area detector, using graphite monochromated MoKα radiation (λ = 0.71073 Å). The determination of crystal class and unit cell parameters was carried out by the SMART program package. The raw frame data were processed using SAINT and SADABS to yield the reflection data file. The structures were solved by using the SHELXTL program. Refinement was performed on F² anisotropically for all non-hydrogen atoms by the full-matrix least-squares method. The hydrogen atoms were placed at the calculated positions and were included in the structure calculation without further refinement of the parameters.

Ethylene polymerization was performed in a 100-mL glass reactor equipped with a magnetic stirrer. After drying the reactor under N₂ atmosphere, toluene was added to the reactor. The solvent was then saturated with a prescribed ethylene pressure. The co-catalyst (MMAO) was added in Al/Ni molar ratios to the reactor via a syringe, the solution was thermostated to the desired temperature and allowed to equilibrate for 10 min. Then, the catalyst solution in toluene was added to the reactor. The polymerization, conducted under 1.2 atm of ethylene pressure, was terminated with 200 mL of a 3% HCl-MeOH solution. The polymers obtained were adequately washed with methanol and dried under vacuum at 50˚C for 6 h.

Analysis of the polyethylene branching by ¹H NMR spectroscopy [27] : branching density, branches/1000C = (CH₃/3)/[(CH + CH₂ + CH₃)/2] × 1000. CH₃ (alkyl methyl, alk-CH₃, m, 0.70 - 0.95 ppm), CH₂ and CH (alk-CH and alk-CH₂, m, ca. 1.00 - 1.45 ppm) refer to the intensities of the methyl, methylene and methine resonances in ¹H NMR spectra.

The monoimine ligand L' (2,4-dibenzhydryl-6-phenylphenylimino)-butanone was prepared from the reaction of 2,4-bis(diphenylmethyl)-6-methylaniline [26] with 5 equiv of 2,3-butadione at 80% yield on multigram scale ( Scheme 1 ). Subsequently, the reaction with 1 equiv of the corresponding aniline led to the formation of the α-diimine ligand L at 95% yields. The reaction of ligand L with 1.1 equiv of (DME)NiBr₂ in CH₂Cl₂ afforded the desired nickel complex Ni at 93% yield ( Scheme 1 ). Compounds were characterized by ¹H and ¹³C NMR spectroscopies, and elemental analysis. In addition, the classic catalyst Ni' [25] was also used for comparison in this study.

Scheme 1. Synthesis of α-diimine ligand L and its nickel complex Ni.

Furthermore, to confirm the molecular structure of catalyst the single crystal of Ni1 was also grown by slow diffusion of n-hexane in dichloromethane, and their molecular structures were confirmed by single-crystal X-ray diffraction analysis ( Figure 1 ). X-ray diffraction data of single crystal was collected at 100 K on a Bruker Smart CCD area detector with graphite monochromated MoK_α radiation (λ = 0.71073 Å). Selected bond lengths (Å) and angles (˚) for Ni are listed in Table 1 . Crystal data, data collection and refinement parameters are listed in Table 2 .

Ni-CH₂Cl₂ has a pseudo-tetrahedral geometry at the Ni center, showing pseudo-C2-symmetry. The crystals exhibit an asymmetrical α-diimine structure and encapsulate a CH₂Cl₂ molecule. Bond lengths and angles are within the expected range for α-diimine, for example, the bond length of N006-C40 [1.291(7) Å] and N007-C41 [1.291(7) Å] have typical imine double bonds character. Its structure is similar to those reported in the literature for a [NiBr₂(α-diimine)] compound characterized by X-ray diffraction, {bis[N,N'-(2,4,6-trimethylphenyl)imino]acenaphthene}dibromonickel Ni' [25] . In fact, the Ni–N bond distances in complex Ni (2.005 and 1.996 Å) are similar to those determined for Ni' (2.021 Å), and the Ni-Br bond distances in complexes Ni and Ni' are almost identical (2.3573 and 2.3317 Å for Ni' vs. 2.323 Å for Ni'). In addition, the N-Ni-Br angles (112.96˚ for complex C1) are also approximate to those for complex C7 (114.4˚). Specifically, the Br01-Ni03-Br02 angle in Ni is more open and measures 117.60(4)˚, while the bite angles of N007-Ni03-N006 are 80.50(19)˚. This asymmetrical dibenzhydryl and phenyl substituted α-diimine ligand may induce a coordination effect in olefin polymerization [9] .

Polymerization of ethylene with Ni activated by MMAO were carried out at various polymerization temperatures and the [Al]/[Ni] ratio for 10 min under 6 atm of ethylene, and the results are listed in Table 3 . At room temperature, the influence of the [Al]/[Ni] with MMAO was investigated by increasing the [Al]/[Ni] molar ratio from 200 to 800 (entries 1 - 3, Table 1 ). The highest activity of 6.45 × 10⁶ g PE/(mol Ni h) and the highest molecular weight of the polymers were achieved with the [Al]/[Ni] ratio of 500 (entry 3, Table 1 ).

^aPolymerization conditions: Ni = 2.8 μmol in CH₂Cl₂ (2 mL); cocatalyst MMAO; solvent = toluene (30 mL); 6 atm of ethylene; time = 10 min. ^b10⁶ g of PE (mol of Ni)⁻¹ h⁻¹. ^cM_n and M_w/M_n determined by GPC, 10⁴ g mol⁻¹. ^dBranching numbers per 1000C were determined by ¹H NMR.

The influence of the polymerization temperature was studied by varying the temperature from 0˚C to 100˚C (entries 4 - 8, Table 1 ). The maximum catalytic activities of complex Ni1 was observed at 50˚C (entry 6, Table 1 ), and the polymerization at 100˚C still gave high catalytic activities on the level of 10⁶ g of PE/(mol Ni h) (entry 8, Table 1 ).

The molecular weights of the polymers were also investigated at various polymerization temperatures from 0˚C to 100˚C (entries 4 - 8, Table 1 ). The polymer obtained by Ni exhibited its highest molecular weight at 25˚C (entry 5, Table 1 ). Subsequent temperature increases resulted in a decrease in the molecular weight accompanied by broadening of the molecular weight distribution. The observation implies that rapid chain transfer occurs at elevated temperatures [9] .

Steric effect of ortho-position in anilinic moiety can be evaluated by comparing Ni and Ni' (entries 6 and 9, Table 1 ). Ni1-MMAO exhibited higher activity and much higher thermal stability than the corresponding methyl substituted Ni' (entries 6 vs 9, Table 1 ), which can be attributed to the steric effect caused by the presence of dibenzhydryl and phenyl groups in the ortho-position [9] . The significantly higher molecular weight of 4.89 × 10⁵ g mol⁻¹ obtained by Ni ( Figure 2 ), as compared to that from Ni', suggests that the presence of bulky dibenzhydryl and phenyl ortho-substituents on the ligand's aryl rings greatly enhances the rate of chain propagation, effectively suppressing chain-transfer reactions [28] .

The branching densities of the polyethylenes obtained were determined using ¹H NMR spectroscopy [29] [30] [31] . The branching densities of 39 - 76 branches per 1000C were increased with polymerization temperature from 0˚C to 100˚C (entries 4 - 8, Table 1 ). In addition, the branching densities were reduced by increasing the steric bulk of the ortho-substituents on the α-diimine ligand, as evidenced by a comparison between Ni and Ni' at 50˚C (entries 6 vs 9, Table 1 ). The observed disparity in microstructure and lower degree of branching density for the sterically bulkier catalysts may be attributed to a relatively higher propensity for ethylene insertion into primary metal alkyl species compared to secondary metal alkyl species [9] .

The branching structures analysis based on ¹³C NMR [20] showed that 56 methyl, 5 ethyl, 3 n-propyl, 2 n-butyl, 1 sec-butyl and 10 longer chains (>C4 branches) exist for the polyethylene produced by complex Ni at 100˚C ( Figure 3(i) , entry 8, Table 1 ). In contrast, only 39 methyl branches were observed for Ni at 0˚C ( Figure 3(ii) , entry 4, Table 1 ).