FORM ATION OF B IS(1, 10-PHENANTHROL INE) CUPROUS COM PL EXES ON M ETALL IC COPPER SURFACE IN AQUEOUS SOL UTION

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1 o l. 12, N o. 4 V JOU RNAL O F INOR GAN IC CH EM ISTR Y D ec., (, ) X -, (Bz) (T s),, IR UV g V IS M S, [Cu (phen) 2 ] + X - g [Cu (phen) 2 ] (CH 3C 4H 6SO 3)C2H 5OH, X2ray Cu g Cu 0 Cu g, Cu g Cu g : 2 FORM ATION OF B IS(1, 10-PHENANTHROL INE) CUPROUS COM PL EXES ON M ETALL IC COPPER SURFACE IN AQUEOUS SOL UTION N ie Chongsh i 3 Gu Y ijun Sun J ie (S hang hai Institu te of O rg anic Chem istry, Ch inese A cad em y of S ciences, S hang hai ) T he fo rm ation of cup rous comp lex on m etallic copper surface in 1, 102phenanth ro line (phen) aqueous so2 lution has been investigated as expo sed in air and in the p resence of common o rganic anions (X - ) such as ben2 zoate (Bz - ) and to luene sulphonate (T s - ). T he comp lexes depo sited on the surface of m etallic copper have been p roved to be rather pure cup rous phenanth ro line comp lexes having the structure [Cu (phen) 2 ]X based on the elem ental analysis, IR, UV gv IS spectro scopy and m ass spectro scopy (FAB ). T he crystal structure of the comp lex [Cu (phen) 2 ] (CH 3C 6H 4SO 3) C 2H 5OH w as determ ined by X2ray diffraction analysiṡ : :, 61, ; : T he w o rk demonstrated that the Cu g ion in the reaction so lution h indered the p rocess of Cu 0 to Cu g and in the m ean2 w h ile accelerated the p rocess of Cu g to Cu g. Keywords: cuprous phenan throline complex copper surface reaction crystal structure In troduction Copper compounds are impo rtan t catalysts fo r the ox idation and oxygenation of o rgan ic compounds bo th in chem ical and b io logical system ṡ R ecen tly, m uch atten tion has been paid to cup rou s phenan th ro line comp lexes in degrading DNA and p rob ing structu re [1 ]. T he b ind2

2 ing and activation of mo lecu lar oxygen of copper comp lexes have been ex ten sively studied. But the system atics in reactivity of copper comp lexesgo 2 system s and the m echan ism in Cug O 2 chem istry still rem ain no t clearly understood [2 ]. Cup rou s comp lexes are mo stly p repared from [Cu (N CM e) 4 ]X becau se of the stab iliza2 tion of copper (g ) ion by M ecn. A stronger ligand such as 1, 102phenan th ro line and Ph3P can sub stitu te m ethyl n itrile ligands. R eduction m ethods are also u sed fo r the p repara2 tion. But in mo st cases, expe2 rim en ts m u st be carried ou t under a n itrogen o r an argon atmo sphere. In ou r study, a conve2 n ien t p reparative m ethod of cup rou s phenan tro line (phen ) comp lexes w as first in troduced starting from m etallic copper. T he reaction w as perfo rm ed in the phen aqueou s so lu tion w ith som e common o rgan ic an ion s (such as carboxylates o r su lfonates) and expo sed in air at room temperatu re. M etallic copper is no t reactive in either w ater o r m ethano l in an oxygen atmo sphere [3 ]. It has been repo rted that, in the p resence o s b ipyridyl ligands, m etallic copper is ox idized in an aqueou s so lu tion, and b inuclear hydroxyb ridged divalen t copper comp lexes are fo rm ed [4 ]. A direct p reparation of Cu 2+ catecho lates from copper and pheno ls can be perfo rm ed in the p res2 ence of O 2 and catalytic amoun t of CuC l [5 ]. Gargano have studied the reactivity of m etallic copper w ith several acidic o rgan ic compounds in the pyridinegm ethano l so lu tion and an oxy2 gen atmo sphere, resu lting in divalen t copper compounds [3 ]. Benzim idazo le reacted w ith m etallic copper and p roduced Cu 2+ b isbenzim idazo late [6 ]. To ou r know ledge, little has been repo rted on the p reparation of air sen sitive cup rou s comp lexes from m etallic copper in the oxygen2con tain ing aqueou s so lu tion. Exper im en ta l Copper surface reaction in aqueous solution A ll so lven ts are of an analytical grade. 1, 102phenan th ro line (phen ) and sodium ben2 zoate (N abz) are of an analytical grade and sodium p 2to luene su lphonate (N at s) is chem i2 cally pure. 1, 102phenan th ro line w as disso lved in distilled w ater fo r: mo lgl, sodi2 um benzoate (N abz), sodium p 2to luene su lphonate (N at s) w ere added respectively in to the so lu tion at abou t mo lgl. Pu re m etallic copper fo il w as cleaned in 20% su lphu ric acid to remove the ox ide on the su rface and rin sed w ith distilled w ater. D ip the cleaned cop2 per fo il steadily in the phen aqueou s so lu tion in the p resence of N abz o r N at s at room tem 2 peratu re. In half a m inu te, the reacted film cou ld be ob served on the su rface of the copper fo il. T he th ickness of the film increases w ith the tim e delay. A fter abou t th ree hou rs, a dark vio let th ick layer of the reaction p roduct w as tigh tly adhered on the su rface. T he fo il w as re2 moved from the so lu tion, then the residual so lu tion w as ab so rbed and dried the fo il in a P 2O 5 vacuum ed desicato r. T he su rface reaction p roduct cou ld be easily separated by disso lving in deoxygenated ethano l at an argon atmo sphere. A fter removing the so lven t by suction, a dark vio let pow der p roduct w as ob tained fo r m easu rem en t w ithou t any fu rther purification. T he p roduct is stab le in dry and inert atmo sphere. Fo r investigating the influence of [Cu (phen ) 2 ] 2+ (Cu ) g on the su rface reaction, w e added differen t amoun ts of CuBz2 3H 2O (in conc. range mo lgl ) to the pheng Bz - so lu tion, in w h ich still on ly the Bz - as an ion w as p resen ṫ A defin ite size (S ) of the cop2

3 4 351 per fo il (w eigh t M ) w as dipped in the so lu tion fo r 2. 7 hou rs, then the fo il w as taken ou t, dried and w eighed together w ith the depo sited cup rou s comp lex film (Cu g ) to ob tain M ȧ T he actual depo sited w eigh t m a= M a- M e, there M e w as the net w eigh t of the copper fo il af2 ter disso lving the depo sited comp lex by ethano l. T he to tal lo ss of the copper fo il w as m (Cu) = M - M ė F ig. 1 show ed m a and m t (the theo retical yield of co rresponding (Cu g ) calcu2 lated from m (Cu) fo r differen t Cu g concen tration s in so lu tion. Spectrocopy and X-ray crysta llography Infrared spectra w ere m easu red w ith a D igilab FT S220E infrared spectrom eter by re2 flection ab so rp tion ( inciden t angle = 80 and 26 ) on the copper fo il sub strate. IR spectra w ere also m easu red by casting the ethano l so2 lu tion of the p ro2 duct on BaF 2 o r KR S25 crystal. T he KB r pel2 let samp ling m ethod is no t alw ays su itab le be2 cau se of the ion exchange. T he UV gv IS spec2 F ig. 1 A ctual depo sited w eigh t m a and theo retical depo sited w eigh t m t on unit area of copper fo il at different concentrations of Cu g, reaction tim e 2. 7 h rs tra w ere reco rded by a Perk in2e lm er L am da25 sp ect rop ho tom eter u sing the deoxygena ted ethano l so lu tion. M ass spectra w ere m easu red u sing the FAB sou rce on a V G Q uattro M S2 spectrom eter. A reddish b row n crystal of [Cu (phen) 2 ] T s C 2H 5OH w as ob tained from the ethano lg to luene so lu tion. A p rism atic crystal having an app rox im ate dim en sion of mm w as moun ted in a glass cap illary. A ll m easu rem en ts w ere carried ou t on a R igaku RA SA 27R diffractrom eter u sing a graph ite monoch rom atized M o2k Α radiation (Κ= ) and a 12 kw ro tating anode X2ray generato r. C rystal data: monoclin ic, space group P 21gc (# 14), a= (2), b= (1), c= (8). Β= (5) and Z= 4, V = 2991 (3) 3, D calc= ggcm 3. Results and D iscuss ion T he su rface depo sition reaction on the m etallic copper su rface is h igh ly repeatab le in the phen aqueou s so lu tion at an am b ien t temperatu re range and in p resence of som e o r2 gan ic salts such as carboxylates o r su lphonates. H ere w e focu s on the resu lts u sing the Bz - and T s - an ion. Sto ich iom etry of the surface reaction products T he su rface reaction p roduct u sing Bz - as an ion show s M L CT ab so rp tion m ax im um at nm and the mo lar ab so rp tivity of w h ich is abou t 6830 mo l - 1 L cm - 1. It is con sis2 ten t w ith the repo rted data [7 ] of [Cu (phen) 2 ] +. IR spectra of the p roduct show phen ab so rp2 tion s at 722 (vs), 839 (m ), 1423 ( s), 1505 (w ), 1561 (vs) cm - 1 and Μas (COO - ) and Μs (COO - ) at 1608 (vs) and 1352 (m ) cm - 1 respectively. T he FAB M S spectrum gives m gz (% ) : 544 ( [Cu (phen) 2 ]Bz +, 5), 439 ( [OCu (phen) 2 ] +, 2), 423 ( [Cu (phen) 2 ] +, 80), 365 ( [Cu (phen) C 6H 5COOH ] +, 10) and 243 ( [Cu (phen ) ] +, 100). E lem en tal analysis of the

4 film p roduct, found: C, ; H, 3. 79; N, C31H 21CuN 4O 2 requ ires fo r C, ; H, 3. 88; N, A ll resu lts suppo rt the mo lecu lar fo rm u la [Cu (phen) 2 ] (C 6H 5COO ) fo r the p roduct availab le. The crysta l structure of [Cu (phen) 2 ]Ts C2H5OH T he crystal structu re of the comp lex is con sisten t w ith the sto ich iom etry and connectivi2 ty expected fo r [Cu (phen) 2 ]T s C 2H 5OH. T he mo lecu le con sists of a monovalen t cation [Cu (phen) 2 ] +, a large an ion CH 3C 6H 4SO 3 - and a nonbonding so lven t C 2H 5OH in the lattice. T he perspective view of the mo lecu le is p resen ted in F ig. 2, together w ith the atom ic num 2 bering schem e. T he selected bond distances and angles are given in T ab le 1. T he coo rdina2 tion around the cup rou s ion is comp leted by fou r n itrogen atom s from tw o phenan th ro line lig2 ands w ith Cu2N bond distances ranging from (3) (2), and N 2Cu2N bond angles abou t 82. Bo th Cu2N distances and N 2Cu2N bond angles are con sisten t w ith crystal struc2 tu re of [Cu (phen) 2 ]C lo 4 and [Cu (phen) 2 ] (CuB r2) repo rted in R ef. 8, w h ich has the sam e cation as that in ou r w o rk. T he in terligand dihedral angle is no t qu ite far from 90, w ith in terligand N 2Cu2N angles differing from to It seem s that differen t an ion affects the in terligand dihedral angles. O u r case is comparab le w ith the structu re of the cation [Cu (phen) 2 ] (CuB r2) w h ich show s the in terligand dihedral angle 76. 8, bu t in con2 trast to that of [Cu (phen) 2 ]C lo 4 w ith T he dihedral angles betw een the p lanar an ion CH 3C 6H 4SO - 3 and the tw o phen ligands in the cation are nearly equal, w h ich are and , resp ect ively. Table 1 Selected A tom ic D istances ( ) and Bond Angles ( ) for [Cu (phen) 2 ]Ts C2H5OH Cu2N (1) (2) Cu2N (2) (3) Cu2N (3) (2) Cu2N (4) (2) C12N (3) (4) C122N (3) C112N (4) C102N (4) C222N (1) C232N (1) C242N (2) C132N (2) (3) (3) (3) (3) (3) (3) (4) N (1) 2Cu2N (2) (9) N (1) 2Cu2N (3) (9) N (1) 2Cu2N (4) (9) N (2) 2Cu2N (3) (9) N (2) 2Cu2N (4) N (3) 2Cu2N (4) Cu2N (1) 2C22 Cu2N (1) 2C23 Cu2N (2) 2C13 Cu2N (2) 2C24 Cu2N (3) 2C1 Cu2N (3) 2C12 Cu2N (4) 2C10 Cu2N (4) 2C (1) 82 (1) 130 (2) 112 (1) 131 (2) 112 (1) 132 (2) 108 (2) 134 (2) 113 (1) Forma tion of the cuprous com plex f ilm on m eta llic copper surface T he depo sition of b is (1, 102phenan th ro line) cup rou s comp lex on the copper su rface in the aqueou s so lu tion, in trin sically is an ox idation reaction of copper by the mo lecu lar oxygen in the p resence of 1, 102phenan th ro line. T he reaction canno t take p lace in a strictly deoxy2 genated so lu tion and an inert atmo sphere. Fo r one dipp ing reaction of a copper fo il, the th ickness of the depo sited cup rou s comp lex film reached the m ax im um (ca. 10 Λm ) after abou t 8 hou rs, yielding abou t m ggcm 2.

5 4 353 F ig. 2 A n OR T EP view of [Cu (phen) 2 ]T s C 2H 5OH, show ing the atom ic num bering L ater, the th ickness began to decrease, becau se the cup rou s comp lex on the fo il began to be ox idized to [Cu (phen) 2 ] 2+ and disso lved in to the so lu tion. A fter abou t tw o days, all depo sit2 ed cup rou s comp lex w as disso lved in to the so lu tion. It imp lies that [Cu (phen) 2 ] 2+ m ay influ2 ence the fo rm ation of [Cu (phen) 2 ]X in the system. T he influence of [Cu (phen) 2 ] 2+ ion to the su rface reaction in the so lu tion are show n in F ig. 1. Cu rve (a) show s m t decreases w ith the increasing concen tration of Cu g in the so lu2 tion. T h is indicates that Cu g ion h inders the ox idation of Cu 0. Bo th the ox idation p rocess Cu 0 Cu g (depo sited on the fo il) and Cu g Cu g (disso lved in to the so lu tion) con tribu te to the copper con sump tion m (Cu). W e cou ld find that m t is no t alw ays equal to actual yield of Cu g m a, generally m a< m t, becau se a part of the depo sited cup rou s comp lex is disso lved by ox idation fo r Cu g. In F ig. 1 w e cou ld find that m aequals to m t w ithou t adding Cu g w ith in at least 2. 7 hou rṡ It imp lies that in several hou rs the su rface reaction has little by2p roduct at very low Cu g ion concen tration. T he mo re the Cu g ion concen tration increases, the mo re m a deviates from m ṫ A nd the yield of the depo sited Cu g sharp ly decreases. A pparen tly a part of the cup rou s comp lex w as disso lved to Cu g by ox idation at a h igher Cu g concen tration. W e suppo se that in ou r reaction system tw o ox idation p rocesses compete in the w ho le

6 p rocess described above. Cu 0 Cu g p rocess is p redom inated in the early stage. It keep s con2 sum ing mo lecu lar oxygen in the so lu tion fo r a rather long tim e (abou t 8 hou rs) till the film th ickness of the su rface p roduct increases to the m ax im um value. lar oxygen penetrates th rough the Cu g p rocess. In th is period the mo lecu2 film reach ing the copper su rface to m ain tain the T he penetration p rocess m igh t be a tran spo rtation of mo lecu lar oxygen by exchang2 ing b inding comp lex [O 2Cu (phen) 2 ] + th rough the Cu g layer to the copper su rface. W hen the Cu g layer w as th ickened to som e ex ten t, the penetration of oxygen becam e slow er than the con sump tion of oxygen in Cu 0 Cu g p rocesṡ in the so lu tion. T hen Cu g Cu g p rocess becam e p redom inated T he basic study on the reaction of copper (g ) comp lex w ith mo lecu lar oxygen is of great impo rtance fo r understanding the pathw ay of oxygen in copper2catalyzed au to ox idation reaction s in bo th chem ical and b io logical system ṡ T he ox idation of 1, 102phenan th ro line cop2 per (g ) comp lex by mo lecu lar oxygen in the aqueou s so lu tion and w ith m any differen t lig2 ands has been investigated in detail by Go ldstein [9, 10 ]. the reduction of mo lecu lar oxygen by [Cu (phen) 2 ] + in term ediate w ith a copper2oxygen bond, i. e. T hey concluded in their research that (Cu g ) p roceeds via the fo rm ation of an via Cu g 2O 2. D epending on the concen tration of Cu g p resen t in the so lu tion, th is tran sien t m ay either react w ith ano ther Cu g o r decom 2 po se to Cu g and O 2, as show n in Eq. (1) and Eq. (2). Cug 2Cu g + O 2 2- (1) Cu g + O 2= Cu g - O 2 Cu g + O 2 - Cu g 2Cu g + O 2 2- (2) Cu g Cu g in ou r system is no t a simp le p rocess. O u r experim en tal resu lts are con sisten t w ith Go ldstein s conclu sion. W hen ex tra mo lecu lar oxygen is p resen t in the so lu tion, tran sien t comp lex Cu g 2O 2 m ay decompo se to Cu g (Eq. 2). W hen the Cu g concen tration be2 com es h igher in the so lu tion, the tran sien t m ay react w ith ano ther Cu g to p roduce Cu g. T he Cu g ion accelerates the ox idation of Cu g to Cu g. Conclus ion T he cup rou s comp lex film cou ld be fo rm ed in the aqueou s so lu tion on a clean m etallic copp er su rface in the p resence of a n it rogen2con ta in ing heterocyclic ligand such a s 1, 102 phenan th ro line and a p roper o rgan ic an ion (Bz - and T s - fo r in stance ). T he depo sited cup rou s comp lex has p roved to have a sligh tly disto rted tetrahedral skeleton [Cu (phen) 2 ] +. W hen the depo sited Cu g film increased to a m ax im um th ickness, it started to be ox idized to cup ric compound. T he Cu g ion in the so lu tion h indered the p rocess of Cu 0 to Cu g, and in the m eanw h ile accelerated the p rocess of Cu g to Cu g. Acknowledgm en t T h is w o rk w as suppo rted by the N ational N atural Science Foundation of Ch ina. ed to P rof. X. L u s enligh ted discussion and w e thank P rof. Z. 2R. the T he autho rs are indebt2 Feng fo r h is help in the experim enṫ

7 4 355 References [1 ]Pyle, A. M., Barton, J. K., in P rogress in Ino rganic Chem istry, Ed. L ippard, S. J., W iley, N ew Yo rk, V o l. 38, p. 413 (1990). [ 2 ] Karlin, K. D., Gultneh, Y., in P rogress in Ino rganic Chem istry, Ed. L ippard, S. J., W iley, N ew Yo rk, V o l, 35, p. 219 (1978). [ 3 ]Gargano, M., R avasio, N., Ro ssi, M., T irip icch io, A., Cam ellini, M. T., J. Chem. S oc., D alton T ranṡ, 921 (1989). [4 ]Beveridge, S. J., W alker, R. W., A usṫ J. Chem., 33, 2331 (1980). [5 ]Capderiille, P., M aum y, M., T etrahed ron L etter, 23, 1577 (1982). [6 ]Xue, G., Zhang, J., Sh i, G., W u, Y., J. Chem. S oc., P erk in T ranṡ g, 33 (1989). [7 ]V o rres, K. S., D utton, F. B., J. A m eṙ Chem. S oc., 2019 (1955). [ 8 ]H ealy, P. C., Engelhardt, L. M., Patrick, V. A., W h ite, A. H., J. Chem. S oc., D alton T ranṡ, 2541 (1985). [ 9 ]Go ldstein, S., Czap sk i, G., E ldick, R. von, Cohen, H., M eyerstein, D., J. P hy ṡ Chem., 95, 1282 (1991). [10 ]Go ldstein S., Czap sk i, G., J. A m er. Chem. S oc., 105, 7276 (1983).