Rapid acquisition of a sixty-carbon fullerene precursor. A new synthetic approach to C60

Article abstract of DOI:10.1016/S0040-4039(02)02341-9

In a new approach towards C₆₀, two C₃-symmetric precursors having all the carbon content and thirteen rings have been assembled in just one step from readily crafted building-blocks through threefold Wittig-Horner coupling.

Full text of DOI:10.1016/S0040-4039(02)02341-9

TETRAHEDRON
LETTERS
Pergamon
Tetrahedron Letters 43 (2002) 9343–9346
Rapid acquisition of a sixty-carbon fullerene precursor.
A new synthetic approach to C60
Goverdhan Mehta* and P. V. V. Srirama Sarma
Department of Organic Chemistry, Indian Institute of Science, Bangalore 560 012, India
Received 25 August 2002; revised 8 October 2002; accepted 18 October 2002
Abstract—In a new approach towards C60, two C3-symmetric precursors having all the carbon content and thirteen rings have
been assembled in just one step from readily crafted building-blocks through threefold Wittig–Horner coupling. © 2002 Published
by Elsevier Science Ltd.
Ever since its conception,1a detection1b and preparative
access,1c C60 1 has enticed the synthetic community as a
formidable synthetic objective.2 Devising a rational syn-
thesis of buckyball C60, involving the generation of 32
rings and establishing 90 CꢀC bond connectivities, is by
any reckoning a major intellectual and experimental
challenge. Not surprisingly, during the past decade,
many groups around the world have mobilised their
ideas and resources in pursuit of a rational synthetic
route to C60 and only a few months ago a synthesis,
culminating in isolable amounts of 1, has been
reported.3 Early synthetic efforts towards C60, emanat-
ing from triindanone derived 2, C45H48,4 and truxenone
derived 3, C42H30,5 were bold and imaginative, but did
not make further headway. In another approach, sev-
eral groups assembled macrocyclic polyalkyne precur-
sors that eject multiple fragments and collapse to C60
on laser desorption/ionisation (LDI) mass spectro-
* Corresponding author.
0040-4039/02/$ - see front matter © 2002 Published by Elsevier Science Ltd.
PII: S0040-4039(02)02341-9

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G. Mehta, P. V. V. S. Sarma / Tetrahedron Letters 43 (2002) 9343–9346
metry.6 However, from a preparative and classical
synthesis perspective, much attention has been
bestowed on C3-symmetric precursor 4, C60H30, which
can undergo unimolecular, 15-fold tandem cyclisation
ers in which the novel hydrocarbon 6, C60H30, occu-
pies a pivotal role and can deliver C60 through
15-fold unimolecular cyclisation (see arrows), forming
alternating five- and six-membered rings on FVP. The
hexadecacyclic hydrocarbon 6 has an interesting pro-
peller shaped topology as indicated by its energy-min-
imised structure (Scheme 1). Retrosynthetic considera-
tions indicated that 6 can be accessed from 7 or its
tribromo derivative 8 through threefold photocyclisa-
tion or intramolecular Heck coupling,9 respectively,
Scheme 1. It was proposed to assemble the key C60
precursors 7 and 8 in one-step through a threefold
Wittig–Horner type reaction of C3-symmetric build-
ing-blocks.
(see arrows) to C60.3,7 Indeed, laser irradiation of 4
+
’
has led to the observation of C60
by mass
spectrometry7d,e and a tris-halo derivative 5 of 4 on
FVP produced isolable3 quantities of 1. The key pre-
cursors 4 and 5 of C60 in turn, have been assembled
through multi-step synthetic sequences.3,7
As part of our8 ongoing interest in the synthesis of
buckyball 1 and its curved fragments (buckybowls),
we have conceived of an approach different from oth-
Scheme 1. Reagents and conditions: (a) For 7. hw, benzene, propylene oxide, I2; (b) for 8 Pd(OAc)2, BnMe3NBr, K2CO3, DMF,
140°C.
Scheme 2. Reagents and conditions: (a) Br2, Fe, 59%; (b) NBS, AIBN, CCl4, 30%; (c) P(OEt)3, 160°C, ꢀ100%.
Scheme 3. Reagents and conditions: (a) isoprene, sealed tube, 175°C, 40%; (b) DDQ, benzene, D, 70%; (c) NBS, (PhCOO)2, CCl4,
80%; (d) (Bu4N)2Cr2O7, CHCl3, D, 86%.

G. Mehta, P. V. V. S. Sarma / Tetrahedron Letters 43 (2002) 9343–9346
9345
Scheme 4. Reagents and conditions: For 7 X=H, (a) NaH, DMF, 4 days, 70%; (b) 10% Pd/C, H2, EtOAc, 60%; (c) 10% Pd/C,
sealed tube, 400°C. For 8 X=Br, (a) NaH, DMF, 70°C, 4 days, 66%.
For the assembly of 7 and 8, C3-symmetric Wittig–
Horner reagents 9/10 and fluoranthene based tetracyclic
aldehyde 1110 were identified as reaction partners and
were prepared from mesitylene 12 and acenaphthene
13, respectively, as shown in Schemes 2 and 3. Gratify-
ingly, threefold coupling between tris-phosphonate
reagent 910 and aldehyde 11 in the presence of NaH was
smooth and led to C3-symmetric all trans-7 as a bright
yellow solid, Scheme 4.10 Formation of 7 was indicated
by its mass spectrum (MALDI-TOF) which showed a
molecular ion at m/z 757.3 amu (M+), calcd for
C60H36=756.93 amu. While 7 was insoluble in most
organic solvents, its 1H NMR spectrum could be
recorded in 1,1,2,2-tetrachloroethane-d2 at 333 K and
the characteristic ABq pattern centred at l 7.38 with
J=16.2 Hz secured the trans disposition of the olefinic
bonds. However, the next critical step, the threefold
oxidative photocyclisation of 7 to the desired C60 pre-
cursor 6, under a variety of conditions, met with
repeated failure, Scheme 1. Attributing this failure to
the inhibition of cis–trans isomerisation in 7, a neces-
sary requirement for its photocyclisation to 6, due to
steric overcrowding by the bulky benzo-fluoranthene
moiety, we considered an alternative possibility. On
catalytic hydrogenation 7 furnished the hexahydro
product 14, with improved solubility in organic solvents
and its 20 line 13C NMR spectrum with signals at l
38.5 (CH2) and 38.2 (CH2) fully secured its structure.10
As planned, 14 was subjected to cyclodehydrogenation
under a variety of conditions (e.g. Pd/C at 400°C), but
only fragmented products like 8-methyl-fluoranthene
were isolated and the desired compound 6 was not
detected.
the structure but the ABq pattern at l 7.12 confirmed
the expected trans disposition of the olefinic bonds.
Tribromo-8 was now subjected to Pd(II) mediated
Heck coupling under elevated temperature and the
expectation was that under such a regime the cis–trans
equilibrium might take place and cyclisation to 6 could
occur.9 However, the outcome once again was disap-
pointing. An obvious option at this stage was to reduce
the olefinic double bonds in 8 to hexahydro-tribromide
15 and then attempt a Heck coupling as was demon-
strated by us recently in similar systems.9
However, the seemingly straightforward reduction of
the double bonds in 8 could not be achieved despite
many efforts. It appears that the high insolubility of
this substrate in most organic solvents is detrimental to
its further evolution and efforts are underway to over-
come this problem.
In short, we have rapidly assembled 7 (C60H36) and 8
(C60H33Br3) having the full carbon content of C60 and
embedding thirteen rings in just one-step through Wit-
tig–Horner reactions on appropriately crafted partners.
Although, the proposed transformation of 7 and 8 to 6
has not been successful so far, the ready availability of
precursors 7 and 8 is significant and provides stimulus
for further efforts towards C60.
Acknowledgements
We would like to thank the SIF at IISc for providing
high field NMR data. One of us (P.V.V.S.S.) thanks
CSIR for the award of a research fellowship.
At this stage, we turned towards 8 with the intent of
effecting Heck coupling. A threefold Horner–Wittig
reaction between the phosphonate ester 1010 and tetra-
cyclic aldehyde 11 in the presence of NaH was slow but
the expected C3-symmetric all trans tribromide 810 was
realised in reasonable yield, Scheme 4. The mass spec-
trum (MALDI-TOF) exhibited the expected peak at
m/z=993.4 (M+), calcd for C60H33Br3=993.6 and the
1H NMR spectrum of this very insoluble material in
1,1,2,2-tetrachloroethane-d2 at 353 K not only secured
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1
(KBr): 3037, 2923, 1584, 1457, 954 cm−1; H NMR (300
MHz, C2D2Cl4, 333 K): l 8.17 (s, 3H), 8.05 (d, 3H,
J=6.6 Hz), 7.98–7.86 (m, 12H), 7.72 (s, 3H), 7.72–7.61
(m, 9H), 7.42 and 7.34 (ABq, 6H, J=16.2 Hz); MS
+
’
(MALDI-TOF): m/z=757.3 (M ), calcd for C60H36=
756.93; 8: mp >350°C, UV (1,1,2,2-tetrachloroethane):
umax 254, 296, 349 and 365 nm; IR (KBr): 3041, 1457,
1
963, 766 cm−1; H NMR (300 MHz, C2D2Cl4, 353 K): l
8.15 (s, 3H), 8.05 (d, 3H, J=6.6 Hz), 7.99–7.86 (m, 12H),
7.70–7.60 (m, 9H), 7.20 and 7.05 (ABq, 6H, J=16.5 Hz);
+
’
MS (MALDI-TOF): m/z=993.4 (M ), calcd for
C60H33Br3=993.6; 14: mp 180°C, IR (KBr): 3040, 2918,
1601, 1456, 769 cm−1 1H NMR (300 MHz, CDCl3): l
;
7.88–7.74 (m, 15H), 7.63–7.57 (m, 9H), 7.09 (d, 3H,
J=6.3 Hz), 6.92 (s, 3H), 2.97 (brs, 12H); 13C NMR (75
MHz, CDCl3): l 141.8 (3C), 141.6 (3C), 139.7 (3C), 137.3
(3C), 137.1 (6C), 132.7 (3C), 130.0 (3C), 128.0 (3C), 127.9
(6C), 126.6 (3C), 126.5 (3C), 126.2 (3C), 121.8 (3C), 121.3
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+
’
(m/z): 762 (M ). Anal. calcd for C60H42: C, 94.45; H,
5.55. Found: C, 94.65; H, 5.58.