Synthesis and reactivity of N-methyl and N-phenyl meso-unsubstituted N-confused porphyrins

Article abstract of DOI:10.1021/jo802040q

(Chemical Equation Presented) Condensations of 1-methyl and 1-phenyl-2,4-pyrroledicarbaldehydes with a tripyrrane in TFA-dichloromethane, followed by oxidation with aqueous FeCl₃, gave novel cross-conjugated meso-unsubstituted N-confused porphyrins (NCPs; 12). These porphyrin analogues showed significant diatropic ring currents that were enhanced upon protonation. Reactions with nickel(II) acetate in refluxing DMF, or palladium(II) acetate in acetonitrile, gave good yields of the corresponding nickel(II) or palladium(II) organometallic derivatives 18 and 19. These complexes were stable and the proton NMR spectra showed slightly increased downfield shifts to the external protons. Addition of TFA resulted in C-protonation at the internal carbon to give aromatic cations that showed the inner CH resonance between -2.5 and -4.0 ppm. The nickel(II) cations 20a and 20b slowly underwent demetalation but the related palladium cations 20c and 20d were quite robust and showed no loss of palladium after 1 week at room temperature. Reaction of NCPs 12 with silver(I) acetate gave silver(III) derivatives 21a and 21b where an oxidation had occurred at C-3 to afford a lactam unit. The silver complexes showed strong diatropic ring currents and porphyrin-like UV-vis spectra with a Soret band near 430 nm. N-Methyl NCP 21a also reacted with gold(III) acetate to give the gold(III) NCP 21c, albeit in low yield, and this species showed similar spectroscopic properties to silver(III) NCP 21a. Syntheses of N-phenyl NCP 12b were accompanied by the formation of the 3-oxo derivative 15b, and the related N-methyl product 16a could also be obtained when the reaction mixtures were oxidized with silver(I) acetate under acidic conditions. The proton NMR spectra for these aromatic NCPs in CDCl₃ show the internal CH shifted upfield to near -6.5 ppm, while the external meso-protons are strongly deshielded giving 4 singlets between 9 and 10 ppm. This study demonstrates that meso-unsubstituted NCPs have unusual reactivity and unique spectroscopic properties, and these results complement and extend the work on the much better known meso-tetraaryl NCPs.

Full text of DOI:10.1021/jo802040q

Synthesis and Reactivity of N-Methyl and N-Phenyl
meso-Unsubstituted N-Confused Porphyrins†
Timothy D. Lash* and Amber L. Von Ruden
Department of Chemistry, Illinois State UniVersity, Normal, Illinois 61790-4160
tdlash@ilstu.edu
ReceiVed September 14, 2008
Condensationsof1-methyland1-phenyl-2,4-pyrroledicarbaldehydeswithatripyrraneinTFA-dichloromethane,
followed by oxidation with aqueous FeCl3, gave novel cross-conjugated meso-unsubstituted N-confused
porphyrins (NCPs; 12). These porphyrin analogues showed significant diatropic ring currents that were
enhanced upon protonation. Reactions with nickel(II) acetate in refluxing DMF, or palladium(II) acetate
in acetonitrile, gave good yields of the corresponding nickel(II) or palladium(II) organometallic derivatives
18 and 19. These complexes were stable and the proton NMR spectra showed slightly increased downfield
shifts to the external protons. Addition of TFA resulted in C-protonation at the internal carbon to give
aromatic cations that showed the inner CH resonance between -2.5 and -4.0 ppm. The nickel(II) cations
20a and 20b slowly underwent demetalation but the related palladium cations 20c and 20d were quite
robust and showed no loss of palladium after 1 week at room temperature. Reaction of NCPs 12 with
silver(I) acetate gave silver(III) derivatives 21a and 21b where an oxidation had occurred at C-3 to
afford a lactam unit. The silver complexes showed strong diatropic ring currents and porphyrin-like UV-vis
spectra with a Soret band near 430 nm. N-Methyl NCP 21a also reacted with gold(III) acetate to give the
gold(III) NCP 21c, albeit in low yield, and this species showed similar spectroscopic properties to silver(III)
NCP 21a. Syntheses of N-phenyl NCP 12b were accompanied by the formation of the 3-oxo derivative
15b, and the related N-methyl product 16a could also be obtained when the reaction mixtures were
oxidized with silver(I) acetate under acidic conditions. The proton NMR spectra for these aromatic NCPs
in CDCl3 show the internal CH shifted upfield to near -6.5 ppm, while the external meso-protons are
strongly deshielded giving 4 singlets between 9 and 10 ppm. This study demonstrates that meso-
unsubstituted NCPs have unusual reactivity and unique spectroscopic properties, and these results
complement and extend the work on the much better known meso-tetraaryl NCPs.
Introduction
true porphyrins by having an inverted pyrrole moiety and a
CNNN arrangement of core atoms.3 NCPs immediately aroused
a great deal of interest due to their aromatic character, the
presence of relatively long wavelength UV-vis absorptions, and
their ability to generate organometallic derivatives under mild
conditions.4 NCPs have two major tautomeric forms, 1 and 2,
that differ in energy by approximately 5 kcal/mol.5 The fully
aromatic tautomer 1 is favored in organic solvents such as
chloroform and the proton NMR spectrum for NCPs in CDCl3
N-confused porphyrins (NCPs; 1) were first reported as
byproducts in Rothemund-type syntheses by two independent
groups in 1994.1,2 These tetrapyrrolic macrocycles differ from
† Part 47 in the series “Conjugated Macrocycles Related to the Porphyrins”.
For part 46, see Lash, T. D.; Colby, D. A.; Idate, A. S.; Davis, R. N. J. Am.
Chem. Soc. 2007, 129, 13800-13801.
(1) Furuta, H.; Asano, T.; Ogawa, T. J. Am. Chem. Soc. 1994, 116, 767–
768.
(2) Chmielewski, P. J.; Latos-Grazynski, L.; Rachlewicz, K.; Glowiak, T.
Angew. Chem., Int. Ed. Engl. 1994, 33, 779–781.
(3) Sessler, J. L. Angew. Chem., Int. Ed. Engl. 1994, 33, 1348–1350.
10.1021/jo802040q CCC: $40.75
Published on Web 11/08/2008
2008 American Chemical Society
J. Org. Chem. 2008, 73, 9417–9425 9417

Lash and Ruden
with Ni(II), Pd(II), and Pt(II),13 and in this respect have
comparable reactivity to NCP tautomer 2. In contrast, benzo-
carbaporphyrins 614 and related carbaporphyrinoids15-17 act as
trianionic ligands, readily forming silver(III) and gold(III)
complexes, and therefore mirror the properties of aromatic NCP
tautomer 1.
The development of a high yielding procedure for synthesiz-
ing meso-tetrasubstituted NCPs18 opened up the field and has
allowed detailed investigations into the reactivity of these
porphyrin isomers.3,19 However, far less work has been con-
ducted on the synthesis and reactivity of meso-unsubstituted
NCPs.20-22 The first synthesis of meso-unsubstituted NCPs
made use of a MacDonald “2 + 2” procedure, but this method
was not suitable for larger scale reactions.20 Porphyrin analogues
like 5 and 6 were synthesized by a “3 + 1” methodology by
reacting tripyrranes 7 with aromatic dialdehydes.23-25 However,
initial attempts to prepare NCPs 8 by reacting 2,4-pyrroledi-
carbaldehydes 9 with tripyrranes under a variety of conditions
afforded mediocre yields of porphyrinoid products (Scheme 1).21
In these reactions, the macrocyclic product is generated as a
dihydro derivative and an oxidation step is required to generate
the final product. In most of the early studies, DDQ was used
for the dehydrogenation step, but this gave very poor results
for NCPs 8. Eventually, washing the reaction solutions with
dilute aqueous solutions of ferric chloride was found to be a
(10) Benzocarbaporphyrins: (a) Lash, T. D.; Hayes, M. J. Angew. Chem.,
Int. Ed. Engl. 1997, 36, 840–842. (b) Lash, T. D.; Hayes, M. J.; Spence, J. D.;
Muckey, M. A.; Ferrence, G. M.; Szczepura, L. F. J. Org. Chem. 2002, 67,
4860–4874. (c) Liu, D.; Lash, T. D. J. Org. Chem. 2003, 68, 1755–1761. (d)
Lash, T. D.; Muckey, M. A.; Hayes, M. J.; Liu, D.; Spence, J. D.; Ferrence,
G. M. J. Org. Chem. 2003, 68, 8558–8570.
(11) Azuliporphyrins: (a) Lash, T. D.; Chaney, S. T. Angew. Chem., Int. Ed.
1997, 36, 839–840. (b) Lash, T. D.; Colby, D. A.; Graham, S. R.; Chaney, S. T.
J. Org. Chem. 2004, 69, 8851–8864. (c) Graham, S. R.; Colby, D. A.; Lash,
T. D. Angew. Chem., Int. Ed. 2002, 41, 1371–1374. (d) Colby, D. A.; Lash,
T. D. Chem.-Eur. J. 2002, 8, 5397–5402. (e) Lash, T. D.; Colby, D. A.; Ferrence,
G. M. Eur. J. Org. Chem. 2003, 4533–4548. (f) Colby, D. A.; Ferrence, G. M.;
Lash, T. D. Angew. Chem., Int. Ed. 2004, 43, 1346–1349.
(12) Tropiporphyrins: (a) Lash, T. D.; Chaney, S. T. Tetrahedron Lett. 1996,
37, 8825–8828. (b) Bergman, K. M.; Ferrence, G. M.; Lash, T. D. J. Org. Chem.
2004, 69, 7888–7897.
shows the presence of a strong diatropic ring current where the
internal CH resonates at -5 ppm, while the external pyrrolic
protons give rise to a series of peaks between 8.5 and 9.0 ppm.
However, in polar aprotic solvents such as DMF and DMSO,
the cross-conjugated tautomer 2 predominates and surprisingly
this form has been characterized by X-ray crystallography.5
Although the diatropicity of 2 is much reduced, the internal
CH is still shifted upfield to 0.76 ppm in proton NMR spectra
run in d6-DMF.5 The less aromatic tautomer of the NCPs can
be trapped by methylation on the external nitrogen.6 In addition,
NCPs form metallo-derivatives 3 that are derived from tautomer
2withdivalentmetalcationssuchasnickel(II)andpalladium(II).2,7
On the other hand, tautomer 1 can act as a trianionic ligand
and form stable organometallic derivatives 4 with metals in
higher oxidation states such as silver(III).8 In parallel with these
studies, the synthesis9-12 and metalation13-16 of carbaporphy-
rinoids such as 5 and 6 have been reported. Azuliporphyrins 5
act as dianionic ligands giving stable organometallic derivatives
(13) (a) Graham, S. R.; Ferrence, G. M.; Lash, T. D. Chem. Commun. 2002,
894–895. (b) Lash, T. D.; Colby, D. A.; Graham, S. R.; Ferrence, G. M.;
Szczepura, L. F. Inorg. Chem. 2003, 42, 7326–7338.
(14) (a) Muckey, M. A.; Szczepura, L. F.; Ferrence, G. M.; Lash, T. D. Inorg.
Chem. 2002, 41, 4840–4842. (b) Lash, T. D.; Colby, D. A.; Szczepura, L. F.
Inorg. Chem. 2004, 43, 5258–5267.
(15) Lash, T. D.; Rasmussen, J. M.; Bergman, K. M.; Colby, D. A. Org.
Lett. 2004, 6, 549–552.
(16) (a) Liu, D.; Lash, T. D. Chem. Commun. 2002, 2426–2427. (b)
Venkatraman, S.; Anand, V. G.; Pushpan, S. K.; Sankar, J.; Chandrashekar, T. K.
Chem. Commun. 2002, 462–463. (c) Liu, D.; Ferrence, G. M.; Lash, T. D. J.
Org. Chem. 2004, 69, 6079–6093. (d) Miyake, K.; Lash, T. D. Chem. Commun.
2004, 178–179. (e) Lash, T. D.; Pokharel, K.; Serling, J. M.; Yant, V. R.;
Ferrence, G. M. Org. Lett. 2007, 9, 2863–2866.
(17) (a) Stepien, M.; Latos-Grazynski, L.; Lash, T. D.; Szterenberg, L. Inorg.
Chem. 2001, 40, 6892–6900. (b) Stepien, M.; Latos-Grazynski, L. Chem.-Eur.
J. 2001, 7, 5113–5117. (c) Stepien, M.; Latos-Grazynski, L. Acc. Chem. Res.
2005, 38, 88–98. (d) Szymanski, J. T.; Lash, T. D. Tetrahedron Lett. 2003, 44,
8613–8616. (e) Lash, T. D.; Szymanski, J. T.; Ferrence, G. M. J. Org. Chem.
2007, 72, 6481–6492.
(4) (a) Latos-Grazynski, L. Core-Modified Heteroanalogues of Porphyrins
and Metalloporphyrins. In The Porphyrin Handbook; Kadish, K. M., Smith,
K. M., Guilard, R., Eds.; Academic Press: San Diego, 2000; Vol. 2, pp 361-
416. (b) Furuta, H.; Maeda, H.; Osuka, A. Chem. Commun. 2002, 1795–1804.
(c) Harvey, J. D.; Ziegler, C. J. Coord. Chem. ReV. 2003, 247, 1–19. (d)
Chmielewski, P. J.; Latos-Grazynski, L. Coord. Chem. ReV. 2005, 249, 2510–
2533.
(5) Furuta, H.; Ishizuka, T.; Osuka, A.; Dejima, H.; Nakagawa, H.; Ishikawa,
Y. J. Am. Chem. Soc. 2001, 123, 6207–6208.
(6) Chmielewski, P. J.; Latos-Grazynski, L. J. Chem. Soc., Perkin Trans. 2
1995, 503–509.
(7) (a) Szterenberg, L.; Latos-Grazynski, L. Inorg. Chem. 1997, 36, 6287–
6291. (b) Furuta, H.; Kubo, N.; Maeda, H.; Ishizuka, T.; Osuka, A.; Nanami,
H.; Ogawa, T. Inorg. Chem. 2000, 39, 5424–5425.
(18) Geier, G. R., III.; Haynes, D. M.; Lindsey, J. S. Org. Lett. 1999, 1,
1455–1458.
(19) Srinivasan, A.; Furuta, H. Acc. Chem. Res. 2005, 38, 10–20.
(20) Liu, B. Y.; Bru¨ckner, C.; Dolphin, D. Chem. Commun. 1996, 2141–
2142.
(21) Lash, T. D.; Richter, D. T.; Shiner, C. M. J. Org. Chem. 1999, 64,
7973–7982.
(8) (a) Furuta, H.; Ogawa, T.; Uwatoko, Y.; Araki, K. Inorg. Chem. 1999,
38, 2676–2682. (b) Furuta, H.; Morimoto, T.; Osuka, A. Org. Lett. 2003, 5,
1427–1430.
(9) Oxybenziporphyrins: (a) Lash, T. D. Angew. Chem., Int. Ed. Engl. 1995,
34, 2533–2535. (b) Lash, T. D.; Chaney, S. T.; Richter, D. T. J. Org. Chem.
1998, 63, 9076–9088. (c) Richter, D. T.; Lash, T. D. Tetrahedron 2001, 57,
3659–3673.
(22) Morimoto, T.; Taniguchi, S.; Osuka, A.; Furuta, H. Eur. J. Org. Chem.
2005, 3887–3890.
(23) Lash, T. D. Synlett 2000, 279–295.
(24) Lash, T. D. Synthesis of Novel Porphyrinoid Chromophores, In The
Porphyrin Handbook; Kadish, K. M., Smith, K. M., Guilard, R., Eds.; Academic
Press: San Diego, 2000; Vol. 2, pp 125-199.
(25) Lash, T. D. Eur. J. Org. Chem. 2007, 5461–5481.
9418 J. Org. Chem. Vol. 73, No. 23, 2008

meso-Unsubstituted N-Confused Porphyrins
SCHEME 1
SCHEME 2
Results and Discussion
The synthesis of N-substituted NCPs 12 by the “3 + 1”
methodology required the availability of pyrrole dialdehydes
13a and 13b. For this work, we adapted procedures developed
by Anderson et al. for the synthesis of 2,4-pyrroledicarbalde-
hydes.29 N-Methylpyrrole had previously been shown to react
with the Vilsmeier reagent to give an imine salt 14a and this
further reacts with dichloromethyl methyl ether, aluminum
chloride and nitromethane to afford, following hydrolysis, the
required dialdehyde 13a (Scheme 2).29 N-Phenylpyrrole was
shown to react similarly to give 1-phenyl-2,4-pyrroledicarbal-
dehyde in 75% yield. Tripyrrane 7 was treated with TFA, diluted
with dichloromethane, and dialdehyde 13a was added. After
stirring the mixture for 16 h at room temperature, the solution
was oxidized by shaking it with 0.1% aqueous ferric chloride
solution in a separatory funnel for 5 min. The crude product
was purified by column chromatography on grade 3 basic
alumina and recrystallized from chloroform-hexanes to give
N-methyl NCP 12a in 39% yield (Scheme 3). Reaction of
N-phenylpyrrole dialdehyde 13b with 7 afforded the corre-
sponding N-phenyl NCP 12b together with an oxidation product
15b. Following careful chromatography on grade 2 neutral
alumina, 13b and 15b were isolated in 17 and 12% yields,
respectively. The formation of lactam-like confused porphy-
rinoids is well precedented in the literature.30,31 A plausible
mechanism involves initial addition of water to the protonated
NCP to give hemiaminal 16, followed by oxidation to give the
oxo-derivative 15 (Scheme 4). As expected, NCPs 12 showed
intermediary diatropic character.
superior oxidation protocol for these syntheses and under
optimized conditions up to 61% yield of NCPs 8 could be
isolated, although 3-unsubstituted NCP 8c was only obtained
in 16% yield.21 More recently, a synthesis of fully unsubstituted
NCP has also been completed.22 It is noteworthy that the meso-
unsubstituted NCPs show significantly larger diatropic ring
currents and the internal CH for NCPs 8 in CDCl3 was observed
near -6.3 ppm.21 The increased diatropicity in 8 can be ascribed
to a flattening out of the macrocycle due to the relief of steric
congestion caused by meso-aryl substitution. NCP 8a was shown
to react with nickel(II) acetate in DMF at 145 °C to give the
nickel(II) complex 10, but this metallo-derivative was somewhat
unstable and showed little aromatic character.21 Addition of TFA
to an NMR solution of 10 in CDCl3 gave a surprising result
where C-protonation at position C-21 occurred to generate an
aromatic species 11. The proton NMR spectrum showed the
internal CH resonance at -4.93 ppm, and the meso-protons
shifted from 7.83-8.68 ppm in 10 to 9.37-10.01 ppm for 11.21
This phenomenon was subsequently demonstrated for Ni(II) and
Cu(II) complexes derived from meso-tetraaryl NCPs as well.26
As the field of N-confused porphyrin chemistry has devel-
oped, remarkable reactivity features, such as the formation of
N-fused porphyrins,27 have been discovered and a profusion of
unusual coordination complexes have been described.19 Nev-
ertheless, very little work has so-far been conducted on meso-
unsubstituted NCPs. These versions of NCPs have the potential
to extend the reactivity studies while complementing the results
obtained for other carbaporphyrinoid systems such as 5 and 6.
In this paper, we describe rational “3 + 1” syntheses of
N-methyl and N-phenyl NCPs 12 and provide details on the
oxidation and metalation of these new porphyrinoids.28
In the proton NMR spectrum for N-methyl tetraphenyl NCP
17 in CDCl3, the internal CH is reported to show up at 0.98
ppm and the NH gives rise to a peak at 3.43 ppm. However, in
the proton NMR spectrum for 12a, the 21-CH gave rise to a
singlet near 1.5 ppm and the NH showed up as a broad peak at
(26) Chmielewski, P. J.; Latos-Grazynski, L.; Schmidt, I. Inorg. Chem. 2000,
39, 5475–5482.
(27) (a) Furuta, H.; Ishizuka, T.; Osuka, A.; Ogawa, T. J. Am. Chem. Soc.
2000, 122, 5748–5757. (b) Toganoh, M.; Ikeda, S.; Furuta, H. Inorg. Chem.
2007, 46, 10003–10015.
(28) These results were presented, in part, at the following meeting: 233rd
National American Chemical Society Meeting, Chicago, IL, March 2007 (Von
Ruden, A. L.; Lash, T. D. Book of Abstracts, ORGN 192).
(29) Anderson, H. J.; Loader, C. E.; Foster, A. Can. J. Chem. 1980, 58,
2527–2530.
(30) Srinivasan, A.; Ishizuka, T.; Osuka, A.; Furuta, H. J. Am. Chem. Soc.
2003, 125, 878–879.
(31) Halide anion binding has recently been demonstrated for a protonated
meso-unsubstituted 3-oxoNCP. See: Furuta, H.; Nanami, H.; Morimoto, T.;
Ogawa, T.; Kra´l, V.; Sessler, J. L.; Lynch, V. Chem. Asian J. 2008, 3, 592–599.
We thank a referee for bringing this paper to our attention.
J. Org. Chem. Vol. 73, No. 23, 2008 9419

Lash and Ruden
SCHEME 3
SCHEME 4
FIGURE 1. Partial 400 MHz proton NMR spectra of N-methyl NCP
12a in CDCl3. (A) Upfield region showing the broad NH peak at 2.75
ppm; the 21-CH overlaps with the triplet at 1.5 ppm. (B) Proton NMR
spectrum run at a slightly different concentration showing the 21-CH
as a broad shoulder. (C) Proton NMR spectrum for the same NMR
solution as A after a D2O shake. The NH peak has been lost and the
21-CH resonance sharpens up and shifts slightly upfield.
calculations indicate that “contributions from the π electrons
of the phenyl ring are significant” for NCPs 1 and 2.34 Therefore,
these subtle interactions are likely to be responsible for the small
upfield shifts of the inner protons for 17 compared to 12a. The
N-phenyl NCP 12b showed the 21-CH resonance at 2.06 ppm
and the NH was identified as a broad peak near 3.9 ppm. The
meso-protons for 12b gave rise to 4 singlets between 7.90 and
8.52 ppm, whereas the equivalent resonances for 12a showed
up between 8.00 and 8.50 ppm. Apart from the meso-proton
that is adjacent to the phenyl group, the resonances for 12a are
further upfield and taken together the diatropic character of 12b
is significantly reduced compared to 12a. The [18]annulene
model for porphyrinoid aromaticity continues to provide valu-
2.75 ppm (Figure 1). A D2O shake showed exchange of the
NH but the 21-CH resonance also sharpened and shifted slightly
upfield (Figure 1C). A similar effect was previously noted for
substituted azuliporphyrins 5.32 The reduced diatropic shift for
the 21-CH resonance in 12a compared to 17 was unexpected,
as the decrease in macrocyclic planarity due to the presence of
meso-substituents would be likely to lead to downfield shifts
for both the NH and 21-CH resonances. However, computational
studies show that the molecular orbitals for meso-tetraphenyl
NCP differ significantly from unsubstituted NCP,33 and DFT
(33) Belair, J. P.; Ziegler, C. J.; Rajesh, C. S.; Modarelli, D. A. J. Phys.
Chem. A 2002, 106, 6445–6451.
(34) Vyas, S.; Hadad, C. M.; Modarelli, D. A. J. Phys. Chem. A 2008, 112,
6533–6549.
(35) (a) Vogel, E.; Ko¨cher, M.; Schmickler, H.; Lex, J. Angew. Chem., Int.
Ed. Engl. 1986, 25, 257–259. (b) Vogel, E.; Haas, W.; Knipp, B.; Lex, J.;
Schmickler, H. Angew. Chem., Int. Ed. Engl. 1988, 27, 406–409.
(32) Lash, T. D.; El-Beck, J. A.; Ferrence, G. M. J. Org. Chem. 2007, 72,
8402–8415.
9420 J. Org. Chem. Vol. 73, No. 23, 2008

meso-Unsubstituted N-Confused Porphyrins
SCHEME 5
able insights into these types of effects.23,35-38 The N-substituted
NCPs are cross-conjugated but it is noteworthy that an 18 π
electron delocalization pathway is present in dipolar resonance
contributors like 12′ (Scheme 3). The required electron-donation
from the confused pyrrolic nitrogen is clearly aided by the more
electron-donating methyl group in 12a compared to the phenyl
unit in 12b. This trend has also been observed for tert-butyl
and phenyl substituted azuliporphyrins 5 (Scheme 5).39 The
azulene moiety in 5 is electron-donating and gives the azuli-
porphyrins a degree of aromatic character due to zwitterionic
resonance contributors 5′ which combine tropylium character
with a carbaporphyrin-like 18π electron delocalization pathway.
Although the shifts for 5 are not as large as those observed for
NCPs 12, the internal CH is still shifted upfield to approximately
3 ppm. In the tert-butylazuliporphyrin 5a, the 21-CH gave a
resonance at 2.9 ppm but the less electron-donating phenyl
moiety in 5b decreased the contribution of canonical form 5′
and gave this singlet at 3.3 ppm. Observations of this type further
emphasize the close relationship of the NCPs, azuliporphyrins
and other carbaporphyrinoid systems.
FIGURE 2. Upfield region of the 400 MHz proton NMR spectrum
2+
for dication 12aH2 in TFA-CDCl3. The broad resonances near 1
ppm correspond to the three internal NHs and the singlet at -2.8 ppm
is due to the 21-CH.
Addition of TFA to NMR solutions of 12a in CDCl3 gave
the corresponding dication 12aH22+, and this showed a greatly
increased diatropic ring current by proton NMR spectroscopy.
The 21-CH resonance shifted upfield to -2.8 ppm and two broad
peaks were observed at 0.9 (1H) and 1.1 ppm (2H) for the three
NHs (Figure 2). The increased diatropic character is due to the
increased favorability of resonance structures like 12′ which are
no longer hampered by charge separation but instead aid in
charge delocalization. Nevertheless, the presence of an electron-
donating methyl group is beneficial. This explains why the shifts
FIGURE 3. UV-vis spectra for NCP 12a. Blue line: free base in 1%
2+
Et3N-CHCl3. Red line: Dication 12aH2 in 1% TFA-CHCl3.
due to the presence of four hydrogen atoms in the macrocyclic
cavity exacerbating the steric effects due to the meso-substit-
uents.
2+
for N-phenyl NCP dication 12bH2 are decreased compared
The UV-vis spectra for 12a showed two moderate absorption
bands at 409 and 420 nm and weaker broadened absorptions
over the visible region (Figure 3). Addition of TFA generated
to 12aH22+, and the 21-CH now gives a signal at -2.05 ppm
that is weakly coupled to the C-3 doublet (J ) 1 Hz) at 8.96
ppm, while the NH resonances are observed at 0.9 (1H) and
1.9 ppm (2H). This effect is also evident in the downfield shifts
for the meso-protons, which show up as 4 singlets between 9.06
and 9.72 ppm for 12aH22+, while three of these values are
shifted upfield to between 8.94 and 9.06 ppm for 12bH22+. Only
the resonance for the meso-proton next to the phenyl moiety is
2+
dication 12aH2 and gave a stronger Soret band at 427 nm
with a shoulder at 453 nm and a series of Q bands between
500 and 800 nm. PhenylNCP 12b showed a similar spectrum
for the free base, with a weakened Soret-like band at 420 nm,
but this again showed a more intense absorption band at 431
2+
nm for the dication 12bH2
.
2+
an outlier, giving rise to a singlet at 9.70 ppm. Dication 17H2
Metalation of the new NCPs 12 was investigated using
nickel(II) and palladium(II) acetate (Scheme 6). The best results
for incorporating nickel(II) were obtained by refluxing 12a or
12b with Ni(OAc)2 in DMF. The earlier work on the synthesis
of 10 had to be carried out at 145 °C because extensive
decomposition occurred at the slightly higher boiling temper-
ature of DMF. However, better yields of nickel(II) derivatives
were obtained under the higher temperature conditions, and
following column chromatography on basic alumina and re-
crystallization, the nickel derivatives 18 were isolated in
76-90% yield. Reactions of 12 with Pd(OAc)2 were carried
in excess TFA-CDCl3 is reported to give a resonance for the
21-CH at -1.57 ppm and three peaks for the NHs at 2.05, 2.91
and 3.25 ppm, so in this case the meso-tetraphenylNCP shows
decreased diatropicity. This can be attributed to the crowding
(36) The validity of this type of interpretation for these types of macrocyclic
systems is generally supported in the literature34,36 and while it is considered to
be a na¨ıve model, theoretical studies also support these interpretations.37
(37) Wannere, C. S.; Corminboeuf, C.; Allen, W. D.; Schaefer, H. F., III.;
Schleyer, P. v. R. Org. Lett. 2005, 7, 1457–1460.
(38) Aihara, J.-i. J. Phys. Chem. A 2008, 112, 5305–5311.
(39) El-Beck, J. A.; Lash, T. D. Eur. J. Org. Chem. 2007, 3981–3990.
J. Org. Chem. Vol. 73, No. 23, 2008 9421

Lash and Ruden
SCHEME 6
FIGURE 4. Partial proton NMR spectrum of palladium complex 19a
in TFA-CDCl3. (A) Spectrum shows an upfield resonance near -3
ppm for the internal CH of the diatropic cation 20c. (B) External pyrrole
and meso-protons are strongly deshielded as expected for this aromatic
species.
attributed to stabilization of the product due to the presence of
a more electron-donating substituent. The protonation of 18 and
19 is reversible, but in the case of nickel(II) derivatives 20a
and 20b slow demetalation occurs over a period of several hours
to give the NCP dications 12H22+. However, the palladium
complexes showed little sign of decomposition even after a week
at room temperature. The nickel derivatives showed larger
upfield shifts for the 21-CH resonance than for the palladium
cations, but the downfield signals for the palladium cations were
more deshielded. In the methyl series, nickel(II) derivative 20a
gave an upfield resonance at -4.01 ppm, compared to -2.97
ppm for palladium complex 20c. However, the five downfield
singlets for 20c fell into the range of 9.56-10.42 ppm compared
to 9.41-10.19 ppm for 20a. These data show that the palladium
cations are more diatropic than the nickel species, and the
differences in the chemical shifts for the 21-CH resonance can
be attributed to the higher electronegativity of Pd compared to
Ni. The phenyl substituted cations 20b and 20d showed a
decreased upfield shift for the 21-CH resonance and a decreased
downfield shift for the meso-proton resonances due to the
reduced electron-donating capabilities of the phenyl substituent.
The UV-vis spectra of the nickel(II) derivatives 18 and
palladium(II) complexes 19 differed considerably from one
another (Figure 5), as had been observed previously for
metalated azuliporphyrins,13,31,39 but the N-methyl and N-phenyl
complexes were very similar in each case. For instance, nickel
derivative 18b gave two stronger absorptions at 342 and 406
nm, together with a shoulder at 454 nm and a prominent peak
at 557 nm. Palladium complex 20b gave a more complex
spectrum with three stronger peaks in the Soret region and a
series of smaller bands between 500 and 750 nm. Addition of
TFA to 18a gave a spectrum with two bands at 327 and 406
nm, and a broad band between 500 and 600 nm, that corresponds
to the aromatic cation 20b (Figure 5A). In the case of 19b,
addition of TFA gave bright green solutions of 20d that showed
a strong broad band at 437 nm and weaker broad absorptions
between 500 and 650 nm (Figure 5B). Again the methyl and
phenyl substituted versions for each metal gave similar UV-vis
absorption spectra.
out in refluxing acetonitrile and the palladium(II) complexes
19 were isolated in 58-63% yield. Unlike the moderately
unstable nickel(II) complex 10, the new nickel and palladium
derivatives were robust and stable in solution for prolonged
periods of time. The proton NMR spectra for 18 and 19 showed
the meso-protons between 8.32 and 8.84 ppm, values that are
significantly downfield from the free base species 12, but these
chemical shifts were similar for the methyl and phenyl series.
The chemical shifts are shifted slightly downfield for the
palladium complexes 19 compared to the nickel derivatives 18,
and this small effect can be attributed to the increased planarity
expected for the organopalladium species.
Addition of a trace amount of TFA to an NMR solution of
18a in CDCl3 showed a large downfield shift to the meso-protons
and the external pyrrole CH, giving five 1H singlets at 9.41,
9.45, 9.61, 9.98, and 10.19 ppm, and a broad upfield resonance
was observed near -4.0 ppm. These observations are consistent
with the formation of an aromatic C-protonated complex 20a.
Further addition of TFA caused the upfield peak to sharpen up
but otherwise did not significantly alter the proton NMR
spectrum. The nickel(II) complex of the 2-phenylNCP (18b)
also showed C-protonation on the internal carbon to give 20b
but it was necessary to add several drops of TFA to resolve the
upfield resonance. The same phenomenon was observed for
palladium(II) complex 19a which also gave C-protonation to
form 20c and like 18b this complex required the addition of
several drops of TFA to show the upfield resonance (Figure 4).
Finally, palladium complex 19b showed no protonation in the
presence of trace amounts of TFA but turned bright green in
the presence of 2 drops of TFA and again showed an upfield
resonance on addition of larger quantities of acid. The trends
show that the nickel(II) complexes undergo protonation more
easily than the palladium derivatives, and the N-methyl com-
plexes react more readily than the N-phenyl species. The
increased reactivity of the N-methyl series can again be
The formation of silver derivatives was also investigated
(Scheme 6). Tetraphenyl NCP8 and many carbaporphyrinoid
9422 J. Org. Chem. Vol. 73, No. 23, 2008

meso-Unsubstituted N-Confused Porphyrins
FIGURE 6. UV-vis spectrum of silver complex 21a in chloroform
(black line). These data are contrasted to the UV-vis spectra of nickel
complex 18a (red line) and palladium complex 19a (green line) which
do not show the strong porphyrin-like Soret band produced by 21a.
present at 1677 cm-1, confirming the presence of a carbonyl
moiety. These data indicate that the product is the silver(III)
lactam-type NCP 21a, and that the silver acetate had acted as
an oxidant as well as a source of silver ions. This is consistent
with the observation that the oxo-derivative 15b was formed
as a byproduct in the synthesis of NCP 12b (Scheme 3).
N-Phenyl NCP 12b also reacted with silver(I) acetate to give
silver(III) complex 21b. In this case, the product was sufficiently
soluble to obtain carbon-13 NMR data in CDCl3, and a
resonance for the carbonyl unit was identified at 169.5 ppm.
The UV-vis spectrum of 21b was slightly red-shifted compared
to 21a, and showed a strong Soret band at 432 nm.
As silver(I) acetate is acting as an oxidant during metalation,
we speculated that it could be used under acidic conditions to
prepare the free base porphyrinoid 15a (Scheme 3). Tripyrrane
7 was reacted with dialdehyde 13a in the presence of TFA in
dichloromethane and then treated with AgOAc. Following
column chromatography and recrystallization, lactam 15a was
isolated in 11% yield. The oxo-species was very aromatic by
proton NMR spectroscopy, although like its silver(III) derivative
15a had poor solubility characteristics. The proton NMR
spectrum of 15a in CDCl3 showed the internal CH strongly
shifted upfield to -6.63 ppm, while the NHs gave a broad 2H
signal centered on -3.9 ppm. The meso-protons produced four
1H singlets in the downfield region at 9.06, 9.64, 9.73, and 9.83
ppm (Figure 7). The presence of a porphyrin-like aromatic ring
current was also supported by the downfield shifts for the
peripheral substituents and the pyrrolic methyl groups gave two
3H singlets at 3.47 and 3.50 ppm. As expected, the UV-vis
spectrum for the free base 15a was porphyrin-like showing two
Soret bands at 421 and 435 nm and Q bands at 517, 556, 607,
and 667 nm. The related N-phenyl oxo-species 15b has similar
spectroscopic properties giving a porphyrin-like UV-vis spec-
trum and a highly diatropic proton NMR spectrum. Addition
of trace amounts of TFA to solutions of 15a or 15b gave the
corresponding cations 15H+. The cations showed similar
diatropic ring currents in their proton NMR spectra and the
UV-vis spectra were still porphyrin-like. The UV-vis spectrum
for 15aH+ in 1% TFA-CDCl3 showed two Soret bands at 427
and 456 nm and a broad band at longer wavelengths. The proton
NMR spectrum of 15aH+ in trace TFA-CDCl3 shows the 21-
CH resonance at -6.46 ppm and three 1H singlets for the NHs
FIGURE 5. (A) UV-vis spectra of nickel complex 18b. Blue line:
metal complex in CHCl3; red line: cation 20b in 5% TFA-chloroform.
(B) UV-vis spectra of palladium complex 19b. Blue line: metal
complex in CHCl3; red line: cation 20d in 5% TFA-chloroform.
systems14-16 easily form silver(III) derivatives, although por-
phyrins generally afford silver(II) complexes.40 N-Methyl NCP
12a was treated with 3 equiv of silver(I) acetate at room
temperature in dichloromethane and following workup and
purification gave a metallo-porphyrinoid product in 65% yield.
The complex was only sparingly soluble in organic solvents
and it was not possible to obtain a carbon-13 NMR spectrum.
However, the proton NMR spectrum in CDCl3 showed only
four 1H singlets at 9.10, 9.65, 9.74, and 9.86 ppm, no evidence
for the presence of an internal NH or CH were observable, and
the 3H singlets corresponding to the two methyl groups were
shifted downfield to 3.48 and 3.50 ppm. These data show that
the silver complex has taken on a fully aromatic carbaporphy-
rinoid structure unlike the nickel and palladium complexes 18
and 19, respectively. The UV-vis spectrum for the silver
complex (Figure 6) showed the presence of a strong Soret band
at 429 nm and a series of Q-type bands that confirm that this
species has porphyrin-like aromatic characteristics. Nevertheless,
the external hydrogen on the confused pyrrole unit has been
lost and HR MS demonstrated that an oxygen atom had been
incorporated and that the molecular formula was C31H34N4OAg.
The IR spectrum showed that a prominent absorption was
(40) Bru¨ckner, C. J. Chem. Educ. 2004, 81, 1665–1669.
J. Org. Chem. Vol. 73, No. 23, 2008 9423

Lash and Ruden
and N-phenyl pyrroledicarbaldehydes. These meso-unsubstituted
NCPs showed intermediary diatropic properties that were
magnified upon protonation in TFA-CDCl3. Reactions with
Ni(OAc)2 or Pd(OAc)2 under mild conditions gave the corre-
sponding nickel(II) and palladium(II) organometallic derivatives,
and all four of these complexes underwent C-protonation to form
an aromatic cation. Reactions with AgOAc gave good yields
of the 3-oxo silver(III) complexes 21a and 21b, where the silver
reagent acts as an oxidant as well as providing the metal cation.
However, reactions with Au(OAc)3 gave poor yields of the
corresponding gold(III) complex 21c. Oxidation of the NCP
macrocycle could also be accomplished without metalation, and
fully aromatic lactam-type NCPs were also isolated and
characterized. This study demonstrates that the chemistry of
meso-unsubstituted NCPs complements and extends the results
obtained for better known carbaporphyrinoids systems such as
the azuliporphyrins and the meso-tetraaryl NCPs.
FIGURE 7. Partial 400 MHz proton NMR spectrum of the N-methyl
NCP lactam 15a in CDCl3 showing the strongly shielded internal CH
at -6.6 ppm and the external meso-protons downfield between 9 and
10 ppm.
Experimental Section
8,12,13,17-Tetraethyl-2,7,18-trimethyl-2-aza-21-carbaporphy-
rin (12a). Tripyrrane dicarboxylic acid 743 (100 mg; 0.22 mmol)
was stirred with TFA (1 mL) under nitrogen for 2 min. The mixture
was diluted with dichloromethane (99 mL) and 1-methyl-2,4-
pyrroledicarbaldehyde (32.8 mg; 0.24 mmol) was immediately
added in a single portion. The resulting solution was stirred
overnight under nitrogen and then washed with water, 0.1% ferric
chloride solution, water, and saturated sodium bicarbonate (the
aqueous solutions were back-extracted with chloroform at each stage
in the extractions). The solvent was removed under reduced pressure
and the residue chromatographed on grade 3 basic alumina, eluting
with 1% methanol-chloroform. The solvent was removed under
reduced pressure and the residue recrystallized from chloroform-
hexanes to yield 2-methyl N-confused porphyrin (39.3 mg; 0.085
mmol; 39%) as dark blue crystals, mp >300 °C; UV-vis (1%
Et3N-CHCl3): λmax (log10ꢀ) 333 (4.69), 409 (4.82), 420 (4.82), 571
(sh, 3.82), 614 (3.96), 657 nm (3.76); UV-vis (1% TFA-CHCl3):
at -3.85, -3.16, and -2.43 ppm. The meso-protons are strongly
shifted into the downfield region showing four 1H singlets at
9.55, 9.89, 10.08, and 10.20 ppm, and the methyl substituents
are also still strongly deshielded giving rise to two 3H singlets
at 3.44 and 3.49 ppm.
λmax (log10ꢀ) 346 (4.66), 427 (4.97), 453 (sh, 4.61), 553 (3.86), 597
In previous studies on the metalation of carbaporphyrinoid
systems, we have demonstrated that gold(III) derivatives of
tetraaryl benzocarbaporphyrins 2214 and oxybenziporphyrins
2341 can easily be prepared using gold(III) acetate as a reagent.
A meso-unsubstituted benzocarbaporphyrin gold(III) complex
was also isolated but very poor yields were obtained in this
case.14 Attempts to prepare gold(III) NCPs from 12a and 12b
gave poor results as well, but the reaction of 12a with Au(OAc)3
in refluxing pyridine did give an 8% yield of the gold complex
21c. The chemical shifts in the proton NMR spectrum of 21c
in CDCl3 were very similar to those obtained for silver(III)
complex 21a, and the UV-vis spectrum of 21c was also
comparable, although the Soret band was split into two peaks
at 419 and 436 nm. Interestingly, the synthesis of a gold(III)
complex of tetraphenyl NCP (4b) has only accomplished very
recently.42 The complex, which is reported to have unique
luminescence properties, had to be prepared from a brominated
intermediate rather than directly from tetraphenyl NCP.42
(3.89), 724 nm (3.75); 1H NMR (CDCl3): δ 1.50 (1H, br s),
1.49-1.54 (6H, 2 overlapping triplets), 1.60 (6H, t, J ) 7.2 Hz),
2.75 (1H, br s), 2.83 (3H, s), 2.84 (3H, s), 3.23-3.30 (4H, 2
overlapping quartets), 3.43 (4H, q, J ) 7.6 Hz), 4.52 (3H, s), 7.98
1
(1H, s), 8.00 (1H, s), 8.28 (1H, s), 8.33 (1H, s), 8.47 (1H, s); H
NMR (TFA-CDCl3, dication): δ -2.80 (1H, s), 0.93 (1H, br s),
1.25 (2H, br s), 1.59 (6H, t, J ) 7.2 Hz), 1.64-1.69 (6H, 2
overlapping triplets), 3.24 (3H, s), 3.25 (3H, s), 3.62-3.72 (8H,
m), 4.78 (3H, s), 8.91 (1H, s), 9.06 (1H, s), 9.08 (1H, s), 9.57 (1H,
s), 9.72 (1H, s); 13C NMR (CDCl3): δ 10.7, 16.5, 16.6, 17.1, 19.1,
19.19, 19.23, 35.2, 92.9, 93.5, 104.1, 113.2, 122.0, 132.4, 136.6,
139.0, 139.3, 140.0, 140.3, 141.3, 141.7; 13C NMR (TFA-CDCl3,
dication): δ 11.22, 11.26, 15.9, 16.7, 19.3, 19.4, 19.5, 37.2, 95.0,
95.4, 104.9, 107.9, 116.8, 123.0, 132.8, 140.8, 141.7, 141.9, 142.1,
142.3, 143.3, 144.7, 145.3, 145.4, 147.1, 147.3, 148.8, 149.6; HR
MS (FAB): Calcd for C31H36N4 + H: 465.3018. Found: 465.3018.
Anal. calcd for C31H36N4 ·1/8CHCl3: C, 77.95; H, 7.59; N, 11.68.
Found: C, 77.77; H, 7.49; N, 11.49.
[8,12,13,17-Tetraethyl-2,7,18-trimethyl-2-aza-21-carbaporphy-
rinato]nickel(II) (18a). Nickel(II) acetate tetrahydrate (12 mg; 0.048
mmol) was added to a solution of 2-methyl N-confused porphyrin
12a (22.0 mg; 0.048 mmol) in DMF (24 mL), and the solution
was stirred under reflux for 30 min. The solution was cooled, diluted
with chloroform, and washed with water. The organic layer was
separated, evaporated to dryness, and the residue chromatographed
on grade 3 basic alumina, eluting with chloroform, to give a dark
red band. The solvent was evaporated and the residue recrystallized
from chloroform-methanol to yield the nickel(II) complex (22.2
mg; 0.043 mmol; 89%) as dark purple crystals, mp >300 °C;
Conclusions
Two examples of cross-conjugated N-confused porphyrins
were prepared by the “3 + 1” methodology using N-methyl
(41) El-Beck, J. A.; Lash, T. D. Org. Lett. 2006, 8, 5263–5266.
(42) Toganoh, M.; Niino, T.; Furuta, H. Chem. Commun. 2008, 4070–4072.
(43) (a) Sessler, J. L.; Johnson, M. R.; Lynch, V. J. Org. Chem. 1987, 52,
4394–4397. (b) Lash, T. D. J. Porphyrins Phthalocyanines 1997, 1, 29–44.
9424 J. Org. Chem. Vol. 73, No. 23, 2008

meso-Unsubstituted N-Confused Porphyrins
UV-vis (CHCl3): λmax (log10ꢀ) 340 (4.95), 405 (4.95), 418 (infl,
4.89), 453 (sh, 4.55), 516 (4.15), 558 (4.51), 710 (3.77), 772 nm
(3.70); UV-vis (5% TFA-CHCl3): λmax (log10ꢀ) 324 (4.84), 407
104.2, 113.4, 120.8, 131.4, 135.6, 136.5, 139.1, 140.1, 142.1, 143.5,
145.1, 146.8, 148.3, 148.6; HR MS (EI): Calcd for C31H34N4Pd:
568.1818 Found: 568.1813. Anal. calcd for C31H34N4Pd·1/5CHCl3:
C, 63.20; H, 5.81; N, 9.45. Found: C, 63.40; H, 5.97; N, 9.07.
Silver(III) Complex of 2-Methyl-3-oxo-N-confused Porphyrin
(21a). Three equivalents of silver(I) acetate (21.5 mg; 0.13 mmol)
were added to a solution of 2-methyl N-confused porphyrin 12a
(20 mg; 0.043 mmol) in dichloromethane (40 mL), and the solution
was stirred at room temperature overnight under nitrogen. The
solution was washed with water, and the organic layer was separated
and evaporated to dryness. The purple residue was chromatographed
on grade 3 basic alumina, eluting with chloroform, and afforded a
dark red band. The solvent was evaporated to dryness and the
residue recrystallized from chloroform-methanol to yield the
silver(III) complex (16.4 mg; 0.028 mmol; 65%) as greenish
metallic crystals, mp >300 °C; UV-vis (CHCl3): λmax (log10ꢀ) 359
(4.50), 432 (5.35), 529 (4.21), 547 (4.38), 568 (4.49), 603 nm (4.44);
UV-vis (1% TFA-CHCl3): λmax (log10ꢀ) 364 (4.56), 429 (5.29),
1
(4.99), 540 nm (4.43); H NMR (CDCl3): δ 1.51-1.56 (6H, m),
1.59-1.64 (6H, m), 2.91 (3H, s), 2.92 (3H, s), 3.32-3.45 (8H,
m), 4.46 (3H, s), 8.37 (1H, s), 8.41 (1H, s), 8.45 (1H, s), 8.52 (1H,
1
s), 8.59 (1H, s); H NMR (TFA-CDCl3): δ -4.01 (1H, br s),
1.63-1.69 (6H, m), 1.72-1.77 (6H, m), 3.20 (3H, s), 3.21 (3H,
s), 3.60-3.74 (8H, m), 5.11 (3H, s), 9.41 (1H, s), 9.45 (1H, s),
9.61 (1H, s), 9.98 (1H, s), 10.19 (1H, s); 13C NMR (CDCl3): δ
10.9, 11.0, 16.4, 16.8, 17.36, 17.43, 19.2, 19.36, 19.41, 35.0, 95.4,
95.9, 101.9, 111.6, 115.5, 123.9, 134.1, 136.8, 137.8, 140.0, 140.7,
142.9, 144.1, 144.4, 144.8, 148.6, 149.8, 151.3, 153.1; HR MS (EI):
Calcd for C31H34N4Ni: 520.2137 Found: 520.2133. Anal. calcd for
C31H34N4Ni·1/5CHCl3: C, 68.73; H, 6.32; N, 10.27. Found: C, 68.77;
H, 6.56; N, 9.99.
[8,12,13,17-Tetraethyl-2,7,18-trimethyl-2-aza-21-carbaporphy-
rinato]palladium(II) (19a). Palladium(II) acetate (26.9 mg; 0.12
mmol) was added to a solution of 2-methyl N-confused porphyrin
12a (55.7 mg; 0.12 mmol) in chloroform (200 mL), and the solution
was stirred under reflux for 30 min. The solution was washed with
water, and the organic layer separated and then evaporated to
dryness. The residue was chromatographed on grade 3 basic
alumina, eluting with chloroform, and the product collected as a
reddish/brown band. The solvent was evaporated to dryness and
recrystallized with chloroform-methanol to yield the palladium(II)
complex (43.0 mg; 0.076 mmol; 63%) as dark purple crystals, mp
>300 °C; UV-vis (CHCl3): λmax (log10ꢀ) 344 (4.91), 415 (4.99),
433 (4.96), 537 (4.22), 567 (4.47), 611 (3.94), 666 (3.98), 728 nm
(3.91); UV-vis (5% TFA-CHCl3): λmax (log10ꢀ) 310 (4.73), 429
1
526 (4.20), 566 (4.42), 599 nm (4.35); IR: νCdO 1677 cm-1; H
NMR (CDCl3): δ 1.77-1.85 (12H, m), 3.48 (3H, s), 3.50 (3H, s),
3.90-4.02 (8H, m), 4.24 (3H, s), 9.10 (1H, s), 9.65 (1H, s), 9.74
(1H, s), 9.86 (1H, s); HR MS (EI): Calcd for C31H34N4OAg:
584.1705. Found: 584.1702. Anal. calcd for C31H34N4OAg ·
1/5CHCl3: C, 61.50; H, 5.49; N, 9.19; Found: C, 61.36; H, 5.52; N,
8.93.
Acknowledgment. This material is based upon work sup-
ported by the National Science Foundation under Grant No.
CHE-0616555 and the Petroleum Research Fund, administered
by the American Chemical Society.
1
(4.92), 602 nm (4.33); H NMR (CDCl3): δ 1.56-1.61 (6H, 2
Supporting Information Available: Experimental proce-
dures for compounds 12b, 13a, 13b, 15a, 15b, 18b, 19b, 21b,
overlapping triplets), 1.62-1.67 (6H, 2 overlapping triplets), 2.98
(3H, s), 2.99 (3H, s), 3.39-3.52 (8H, m), 4.48 (3H, s), 8.41 (1H,
s), 8.46 (1H, s), 8.488 (1H, s), 8.492 (1H, s), 8.65 (1H, s); 1H NMR
(TFA-CDCl3): δ -2.97 (1H, br s), 1.73-1.83 (12H, m), 3.31 (6H,
s), 3.73-3.83 (8H, m), 5.17 (3H, s), 9.56 (1H, s), 9.64 (1H, s),
9.81 (1H, s), 9.84 (1H, s), 10.42 (1H, s); 13C NMR (CDCl3): δ
10.8, 10.9, 16.3, 16.6, 17.3, 19.1, 19.2, 19.4, 19.5, 35.0, 96.1, 96.4,
1
and 21c, and MS, UV-vis, H NMR, and 13C NMR spectra
for selected compounds, are provided. This material is available
free of charge via the Internet at http://pubs.acs.org.
JO802040Q
J. Org. Chem. Vol. 73, No. 23, 2008 9425