Synthesis of a 2,2'-Bipyridyl Functionalized Oligovinylene-Phenylene Using Heck and Horner-Wadsworth-Emmons Reactions and X-ray Crystal Structure of E-(4-(4-Bromostyryl)phenyl)(methyl)sulfane

The synthesis of a new 2,2'-bipyridyl functionalized oligovinylenephenylene (OVP-5) containing a methyl protected thiol using Heck coupling and the Horner-Wadsworth-Emmons reaction and is described. A key step involving a diisopropylcarbodiimide promoted dehydration of a stable β-hydroxyphosphonate intermediate was identified. The structure of precursor E-(4-(4-bromostyryl)phenyl)(methyl)sulfane (1) was determined using X-ray crystallography.


Introduction
Oligovinylphenylenes (OVPs) are conjugated molecules that have demonstrated application in optoelectronics [1], molecular devices [2,3], photonics [4], liquid crystals [5] and organic dye sensitizers [6]. Trammell and co-workers recently described a new strategy for the formation of self-assembled monolayers of quinones derived from OVPs with thiol and 2,5-dimethoxylaryl head groups. Attachment of the thiol functionalized OVP to a gold surface allowed the study of formal redox potentials and reaction rates [7].
2,2'-Bipyridine ligands have been used extensively in homogeneous catalysis [8][9][10][11][12][13][14]. Martell and co-workers showed early on that 2,2'-bipyridine Cu(II) complexes are among the most efficient in hydrolyzing selected phosphorofluoridates, a class of compounds closely related to phosphate esters [15]. Since then, another group has reported comprehensively on the hydrolysis of other phosphate esters with such complexes [16]. Recent work by Chang's group showed that immobilized copper(II)bipyridine complexes were even more efficient at hydrolysis than the soluble complexes [17]. For example, a copper-containing polymer prepared by free radical polymerization of a copper(II)vinylbipyridine complex with trimethylolpropane trimethacrylate (TRIM) showed significantly enhanced hydrolysis over the free complexes [17].
We recently initiated a program to investigate copper(II)-bipyridine functionalized molecular wires attached to gold nanoparticles with a view to the modulation of electronic and desolvation effects on catalytic phosphodiester hydrolysis ( Figure 1). We propose that the electronic withdrawing properties of a highly fluorinated OVP ligand attached to a gold nanoparticle as shown, is likely to result in decreased electron density of a neighboring copper(II)-bipyridine functionalized molecular wire, in turn resulting in increased Lewis acidity of coordinated copper ion and consequent increase in catalytic activity. Herein we report the synthesis and characterization of a 2,2'-bipyridine functionalized OVP ligand containing a protected thiol and the X-ray crystal structure of a synthetic precursor E-(4-(4-bromostyryl)phenyl)(methyl)sulfane.

Results and Discussion
Numerous strategies are available for the construction of OVPs. Our synthetic approach to a bipyridine functionalized molecular wire involved a sequential palladium catalyzed Heck coupling and a modified Horner-Wadsworth-Emmons reaction, as shown in Scheme 1. The arylbromide precursor 1 was synthesized, and the yield improved, using a modification of the literature procedure [6] via the reaction of diethyl 4-bromobenzylphosphonate with 4-(methylthiol)benzaldehyde which gave 1 as a spectroscopically pure amorphous solid. Crystallization of a portion of 1 from dichloromethane yielded colorless crystals which were of sufficient quality to be used directly for X-ray structure analysis.

Scheme 1. Synthesis of OVP-5.
The molecule crystallizes on a center of symmetry and therefore only half the molecule is present in the asymmetric unit. Because of this, the bromine atom and the CH 3 S-group are present at half-occupancy. The ORTEP representation of 1 is shown in Figure 2. X-ray analysis confirms the E-stereochemistry previously suggested from the 1 H-NMR spectrum [6].
A palladium catalyzed Heck reaction with Pd 2 (dba) 3 ·CHCl 3 /P t Bu 3 /NEt 3 in dioxane was used to couple 1 with 4-vinylbenzylphosphonate (2) using conditions that are expected to give a high E/Z stereochemical ratio (Scheme 1) [18]. The OVP phosphonate OVP-3 was isolated from the reaction mixture following silica gel flash column chromatography as a yellow solid in 70% yield and identified using 1 H-NMR spectroscopy and mass spectrometry. Only the E-isomer was observed based on the presence of the characteristic AB pattern with coupling constants ~16.0 Hz. Both compound 1 and 4-vinylbenzylphosphonate are recovered from the reaction mixture with no other species being identified. Modifications of the palladium catalyzed coupling reaction were then examined in an attempt to improve the yield of OVP-3, including a ligand-free Heck reaction with dimethylglycine as a promoter [19], the use of Pd(OAc) 2 with Buchwald's ligand, MePhos (2-(dicyclohexylphosphino)-2',4',6'-triisopropylbiphenyl) [20], and decreasing the mol% of palladium catalyst. In each case, no product OVP-3 was observed.
Reaction of the benzylphosphonate OVP-3 with 2,2'-bipyridine-5-carbaldehyde 4 under Horner-Wadsworth-Emmons conditions with an excess of potassium t-butoxide followed by dehydration of the -hydroxyphosphonate intermediate 6 (Schemes 1 and 2) with diisopropylcarbodiimide (DIC) gave OVP-5. Evidence for 6 was provided by in situ 1 H-NMR spectroscopy and the intermediate was not further purified.
The phosphonic acid ethyl ester protons of 6 resonate at 1.41 and 4.01 ppm for the methyl and methylene protons respectively with associated coupling to the phosphorus nucleus. These values are typical for those previously reported for -hydroxyphosphonic acid diethyl esters. We have tentatively assigned a multiplet and doublet (J HP = 28 Hz) at 5.37 and 2.91 ppm to single protons alpha to the -OH and -PO 3 Et 2 groups respectively. The formation of a stable, isolable -hydroxyphosphonate intermediate in the HWE reaction is not entirely unexpected, as a carbanion-stabilizing group in the -position is a requirement for elimination of phosphate from intermediate 8 and formation of an alkene. Compound 6 does not possess a withdrawing group in the -position and cannot undergo elimination.
Reichwein and Pagenkopf recently reported the saponification of -hydroxyphosphonic acid dimethyl esters followed by diisopropylcarbodiimide (DIC) dehydration to give the corresponding olefins [21]. We have discovered that the one-pot reaction of the phosphonic acid diethyl ester OVP-3 with an excess of potassium t-butoxide directly followed by dehydration with DIC in CHCl 3 resulted in conversion to the desired 2,2'-bipyridyl functionalized oligovinylphenylene OVP-5 via intermediate 6 (Scheme 2). We tentatively suggest that excess t-butoxide anion is responsible for monodealkylation of the phosphonic acid ester OVP-3 [2] to give 6 which then undergoes dehydration with the carbodiimide. Compound OVP-5 was identified with 1 H-NMR spectroscopy and ESI mass spectrometry. In situ 1 H-NMR analysis of the DIC dehydration reaction shows complete disappearance of hydrogen atoms  to both hydroxy and phosphonate groups.

General
All reactions were conducted under N 2 using standard Schlenk line and catheter-tubing techniques unless otherwise stated. All 1 H, 31 P and 13 C-NMR spectra were recorded on a Bruker 400 MHz NMR spectrometer and referenced to internal tetramethylsilane. 31 P-NMR spectra were referenced to external H 3 PO 4 . Mass spectra were recorded on a Jeol AccuTOF JMS-T100LC mass spectrometer in ESI or DART mode, or were performed by HT Labs, San Diego, CA, USA. Solvents were obtained as follows and used without further purification: t-butanol, anhydrous dioxane, dimethylformamide (Sigma-Aldrich), acetone, methanol, dichloromethane (Fisher), and CDCl 3 , (Cambridge Isotope Laboratories). Silica gel (60-230 mesh, Sigma-Aldrich) and anhydrous MgSO 4 (Fisher) were used as received. Flash chromatography was performed using silica gel (60-230 mesh, 60Å). TLC was performed on SiO 2 plates with fluorescent indicator. Compounds were visualized under UV light or with phosphomolybdic acid stain. Reagents were obtained as follows and used without further purification: triethylamine, diisopropylcarbodiimide, 4-methylthiobenzaldehyde, 4-vinylbenzyl-phosphonate, Pd 2 (dba)·CHCl 3 (Sigma-Aldrich), P t Bu 3 , potassium t-butoxide (Fisher). Diethyl (4-bromobenzyl)phosphonate was synthesized according to the literature procedure [6].

OVP-5.
A 50 mL Schlenk flask was charged with a solution of 4 (18.4 mg, 0.100 mmol) and OVP-3 (23.9 mg, 0.0500 mmol) in DMF (5.5 mL). The reaction flask was placed in an ice bath, and a solution of t-BuOK (0.0283 g, 0.257 mmol) in t-BuOH (3 mL) was slowly added with stirring. The solutions was allowed to warm to room temperature and stirred for 19 h. Then, CH 2 Cl 2 (20 mL) was added and the reaction mixture was washed with water (4 × 20 mL). The organic layer was dried over MgSO 4 and the solvent was evaporated to give 6 which was identified by 1 H-NMR. Chloroform (0.5 mL) was added followed by DIC (0.0114 g, 90.0 mol). The mixture was stirred for 4 h, filtered on a short silica gel plug and the solvent removed by rotary evaporation to give OVP-5 (47.8 mg, 100%). 1

Conclusions
In summary, a new 2,2'-bipyridine functionalized OVP ligand with a protected thiol has been synthesized using a combination of Horner-Wadsworth-Emmons and palladium catalyzed Heck coupling reactions. Coordination of the ligand to copper(II), and attachment to gold nanoparticles will be reported in due course.