Synthesis and luminescence properties of nine novel carbazolyl diacylhydrazone Schiff-bases

Article abstract of DOI:10.5562/cca2349

Nine novel carbazolyl diacylhydrazone Schiff-bases were synthesized by alkylation, F-C acylation and condensation reactions starting from carbazole and hydrazide. The title Schiff-bases were characterized by ¹H NMR, MS, IR and elemental analysis. The synthetic conditions were optimized, and the best yield of the title Schiff-bases was up to 92.3%. The relationships between the luminescence properties and the structures of the title Schiff-bases were studied. The results showed that the introduction of the Naphthalene-2-yloxy could form great plane conjugate structure to improve their luminescence properties.

Full text of DOI:10.5562/cca2349

CROATICA CHEMICA ACTA
CCACAA, ISSN 0011-1643, e-ISSN 1334-417X
Croat. Chem. Acta 88 (1) (2015) 1–6.
http://dx.doi.org/10.5562/cca2349
Original Scientific Article
Synthesis and Luminescence Properties of Nine Novel
†
Carbazolyl Diacylhydrazone Schiff-bases
*
Limin Wu, Panliang Wu, Dongcai Guo, Wenqiang Fu, Dong Li, and Tao Luo
Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China
RECEIVED AUGUST 1, 2013; REVISED MAY 19, 2014; ACCEPTED NOVEMBER 6, 2014
Abstract. Nine novel carbazolyl diacylhydrazone Schiff-bases were synthesized by alkylation, F-C acyla-
tion and condensation reactions starting from carbazole and hydrazide. The title Schiff-bases were charac-
1
terized by H NMR, MS, IR and elemental analysis. The synthetic conditions were optimized, and the best
yield of the title Schiff-bases was up to 92.3 %. The relationships between the luminescence properties
and the structures of the title Schiff-bases were studied. The results showed that the introduction of the
Naphthalene-2-yloxy could form great plane conjugate structure to improve their luminescence properties.
Keywords: Schiff-bases, carbazole, diacylhydrazone, synthesis, optimize, luminescence property
INTRODUCTION
1
0
ultraviolet spectral region and blue-light emission. The
conjugated π bonds, existed both in acylhydrazone and
carbazole, possess a strong ability in energy transfer.
However, carbazole has never been used to synthesize
the diacylhydrazone Schiff-bases. In this study, we
developed nine novel carbazolyl diacylhydrazone
Schiff-bases by alkylation, F-C acylation and condensa-
tion reactions starting from carbazole and hydrazide.
The hydrogen atom of carbonyl and carbazolyl were
As a peculiar Schiff-base, acylhydrazone have received
great attention for its strong p-π conjugated system,
various coordination forms, strong coordination abili-
1
–5
6
ties, good biological activity, catalytic activity and
fluorescence property7 in recent years. The strong
conjugated system and high intramolecular electron
transfer efficiency of carbazole make it have potential
application prospect in electroluminescence (EL) and
,8
9
11
photoluminescence (PL). Carbazole derivatives repre-
replaced by several different groups to clarify the
sent one of the most widespread class of hole-
transporting materials with strong absorption in the
influence of the substituents on the luminescence prop-
erties of the Schiff-bases (Scheme 1).
Scheme 1. Synthesis route of carbazolyl diacylhydrazone Schiff-bases.
†
th
Dedicated to Professor Mirjana Eckert Maksić on the occasion of her 70 birthday.
Author to whom correspondence should be addressed. (E-mail: dcguo2001@hnu.edu.cn)
*

2
L. Wu et al., Carbazolyl Diacylhydrazone Schiff-bases
EXPERIMENTAL
dropwise to it in an ice bath. The reaction was carried
out in the ice bath for 2 h and further stirred at room
temperature for 48h. The reaction mixture was then
poured into ice water (400 mL) with vigorous stirring to
get a pale-yellow precipitate. The crude products were
filtered, washed with water, dried, and then recrystal-
lized from alcohol to get compound 2.13
All the chemicals used were of analytical grade and
received from commercial suppliers. Solvents were
dried before use. Melting points (m.p.) were determined
on a XT-4 melting point apparatus (Beijing City) and
uncorrected. Elemental analysis (C, H, N) data was
obtained using a Vario-EI-III elemental analyzer (Ge-
many). The IR spectra (KBr) were recorded on a Perkin-
Elemer Spectrum One spectrophotometer in the range of
3,6-diacetyl-9-ethylcarbazole (2a) was synthesised
from acetyl chloride and 1a. A yellow solid (1.80 mmol,
o
90 %). m.p 180–182 C. MS (EI): m/z (%) = 221 (27),
–
1
4
00–4000 cm . UV spectra were obtained on a Lab-
264 (100), 279 (45).
Tech UV-2100 UV Visible spectrophotometer in the
range of 190–450 nm using absolute alcohol as the
solvent and internal reference. The 1H NMR spectra in
3,6-diacetyl-9-proplycarbazole (2b) was synthe-
sised from acetyl chloride and 1b. A pale-yellow solid
(1.70 mmol, 85 %). m.p 165–167 C. MS (EI): m/z (%)
o
CDCl
3
were recorded on a high resolution NMR
= 279 (8), 294 (M+1, 100), 295 (20).
spectrometer (Varian-400) using TMS as an internal
reference. Florescence spectra were carried out at room
temperature on a HITACHI F-2700 fluophotometer.
3,6-diacetyl-9-butylcarbazole (2c) was synthesised
from acetyl chloride and 1c. A pale-yellow solid (1.66
mmol, 83 %). m.p 127–128 C. MS (EI): m/z (%) = 279
o
(
5), 308 (M+1, 100), 308 (23).
General Synthetic Procedure of N-alkyl Carbazole
(
1a–c)
Synthetic Procedure of Ethyl β-naphthyloxyacetate
Carbazole (1.67 g, 10 mmol), tetrabutyl ammonium
bromide (0.32 g, 1 mmol) and potassium hydroxide
Ethyl bromoacetate (5.00 g, 30 mmol) , β-naphthol
(4.30 g, 30 mmol) in acetone (15 mL) and sodium
carbonate anhydrous (6.20 g, 45 mmol) were added to a
100 mL single aperture flask with constant stirring. The
solution was refluxed for 14 h under an anhydrous con-
dition. After standing overnight, the mixture was fil-
tered, washed with cold water (50 mL) several times,
neutralized to pH 7–8 with 10 % NaOH, and extracted
with ether (40 mL) two times. The ether layer collected
was dried by sodium sulfate (4.00 g), and then filtered
after standing for 48 h. Then the filtrate was evaporated
to remove the ether. The product was not characterized
and applied directly to the next step reaction.14
(
2.24 g, 40 mmol) dissolved in acetone (20 mL) were
added to a 100 mL three-necked flask, the mixture
solution was stirred for 40 minutes. Alkyl bromide
(
12 mmol) was added dropwise to the solution with
constant stirring. The mixture was refluxed for 1 h.
The reaction mixture was then poured into ice water
(300 mL) with vigorous stirring to obtain a great deal of
deposit. The mixture was filtered, washed with water
and the filter cake obtained was then recrystallized from
alcohol and water to give N-alkyl carbazole (1a–1c).12
N-ethylcarbazole (1a) was synthesised from bro-
moethane and carbazole. A whitish needle crystals
o
product (9.2 mmol, 92 %). m.p 67.0–68.5 C. MS (EI):
Synthetic Procedure of Methyl p-Nitrobenzoate
m/z (%) = 152 (15), 180 (100), 195 (M, 60).
p-Nitrobenzoic acid (1.67 g, 10 mmol) and methanol
N-proplycarbazole (1b) was synthesised from
bromopropane and carbazole. A whitish needle crystals
(
10 mmol) were added to a 50 mL single aperture flask.
o
To the solution concentrated sulphuric acid (2 mL) was
then added dropwise slowly. The mixture was refluxed
for 12 h and poured into ice water, getting lots of white
solid. The coarse product was filtered, recrystallized
from 50 % alcohol to get a white product, applied
directly to the next step reaction.14
product (8.0 mmol, 80 %). m.p 49–51 C. MS (EI):
m/z (%) = 152 (20), 180 (100), 209 (M, 28).
N-butylcarbazole (1c) was synthesised from bro-
mobutane and carbazole. A whitish needle crystals
o
product (8.5 mmol, 85 %). m.p 57.5–59 C. MS (EI):
m/z (%) = 152 (15), 180 (100), 223 (M, 30).
General Synthetic Procedure of 3,6-Diacetyl-9-alkyl
Carbazole (2a–c)
General Synthetic Procedure of Hydrazide (3a−d)
Appropriate ester (10 mmol) was dissolved in anhydrous
ethanol (25 mL) in a 100 mL single aperture flask with
constant stirring; 85 % hydrazine hydrate (3 mL) was
added dropwise to it. The solution was heated to reflux
for 1 h, cooled down to the room temperature and then
diluted with 100 mL distilled water to get a large white
precipitates. The mixture was filtered, washed with
Aluminium chloride powder (1.10 g, 8 mmol) was dis-
solved partly in dichloromethane (10 mL) in a 100 mL
three-necked flask with constant stirring until the
solution became orange-yellow. To the solution acetyl
chloride (1 mL, 10 mmol) in dichloromethane and
compound 1 (2 mmol) in dichloromethane was added
Croat. Chem. Acta 88 (2015) 1.

L. Wu et al., Carbazolyl Diacylhydrazone Schiff-bases
3
water, dried, and recrystallized from anhydrous ethanol
to get the title compound 3.
C
42
H
37
N
5
O
2
: C, 74.65; H, 5.52; N, 10.30. Found: C,
1
4
74.63; H, 5.74; N, 10.26.
β-naphthyloxyacethydrazide (3a) was synthesised
by the condensation of 85 % hydrazine hydrate with
(
(
Naphthalen-2-yloxy)-acetic Acid {1-[6-(1-{[2-
naphthalen-2-yloxy)-acetyl]-hydrazono}-ethyl)-9-
β-naphthyloxyacetate. A white solid (7.5 mmol, 75 %).
propyl-9H-carbazol-3-yl]-ethylidene}-hydrazide (L
L
A pale-yellow solid (0.752 mmol, 75.2 %). m.p
2
2
1
2
)
1
m.p 173−175 °C. H NMR (400 MHz, DMSO-d
6
):
2
was synthesized by the condensation of 2b with 3a.
δ / ppm = 4.37 (s, 2H), 4.61 (s, 2H), 7.24~7.25 (d, 1H,
J = 4Hz), 7.26~7.29 (t, 1H, J = 1.6 Hz), 7.35~7.38 (d,
H, J = 8Hz), 7.45~7.49 (d, 1H, J = 8.4Hz), 7.77~7.79
d, 1H, J = 8Hz), 7.84~7.86 (t, 2H, J = 3.2Hz), 9.44 (s,
H).
Benzoyl hydrazine (3b) was synthesised by the
condensation of 85 % hydrazine hydrate with ethyl
benzoate. A white solid (7.5 mmol, 75 %). m.p
10.5−113 °C. MS (ESI): m/z (%) = 136 (M, 100), 158
46), 159 (5), 235 (20), 277 (6).
Salicylhydrazide (3c) was synthesized by the
condensation of 85 % hydrazine hydrate with methyl
salicylate. A white solid (8.7 mmol, 87 %). m.p
36−238 °C. IR (KBr):  / cm−1 = 3443, 3055, 2955,
1
(
1
922, 2853, 1661, 1628, 1600, 1549, 1470, 1256, 1122,
1
072, 1065, 952, 739, 701. H NMR (400 MHz,
DMSO-d
Hz, ArH), 8.15 (q, 2H, J = 3.6 Hz, ArH), 7.85 (m, 6H,
ArH), 7.65 (d, 2H, J = 4 Hz, ArH), 7.42 (m, 2H, ArH),
.31 (m, 6H, ArH), 5.38 (m, 2H, CH ), 4.42 (m, 2H,
CH ), 2.40 (s, 6H, N=C−CH ), 1.82 (s, 4H, CH ), 0.86
t, 3H, CH ). MS (EI): m/z (%) = 690 (M+1, 8), 689 (M,
2), 490 (11), 262 (13), 201 (13), 144 (100). Anal.
: C, 74.87; H, 5.70; N, 10.15.
Found: C, 74.53; H, 5.60; N, 9.84.
6
): δ/ppm = 10.81 (s, 2H, NH), 8.75 (d, 2H, J =
4
7
2
1
(
2
3
2
(
1
3
39 5 2
Calcd for C43H N O
1
1
46~147.5 °C. MS (ESI): m/z (%) = 121 (21), 134 (8),
53 (M+1, 100), 154 (5), 175 (10).
p-Nitrobenzoylhydrazine (3d) was synthesized by
the condensation of 85 % hydrazine hydrate with methyl
(
(
Naphthalen-2-yloxy)-acetic Acid {1-[9-butyl-6-(1-{[2-
naphthalen-2-yloxy)-acetyl]-hydrazono}-ethyl)-9H-
carbazol-3-yl]-ethylidene}-hydrazide (L
was synthesized by the condensation of 2c with 3a.
A pale-yellow solid (0.735 mmol, 73.5 %). m.p
3
)
p-nitrobenzoate. A white solid (8.3 mmol, 83 %). m.p
L
3
1
2
8
08−209 °C. H NMR (400 MHz, DMSO-d
6
): δ/ppm =
.21~8.42 (m, 4H), 9.01 (s, 1H), 4.36 (m, 2H).
−1
2
2
1
30−232 °C. IR (KBr):  / cm = 3415, 3054, 2955,
927, 2872, .1683, 1629, 1599, 1509, 1466, 1255, 1122,
General Synthetic Procedure of the Title Schiff-bases
− L
1
070, 1070, 961, 744, 700. H NMR (400 MHz,
(
L
1
9
)
DMSO-d
J = 11 Hz, ArH), 8.11 (d, 2H, J = 6 Hz, ArH), 8.04 (t,
H, J = 7.5 Hz, ArH), 7.85 (m, 4H, ArH), 7.71 (t, 2H,
J = 9 Hz, ArH), 7.65 (d, 2H, J = 9 Hz, ArH), 7.43 (t,
6
): δ / ppm = 10.85 (s, 2H, NH), 8.74 (d, 2H,
The synthesis of Schiff-bases was performed according
to the Scheme 1. Compound 2 (1 mmol) and the hydra-
zide 3 (2.2 mol) were dissolved in ethanol (10 mL) in a
2
4
5
6
4
H, J = 7.5 Hz, ArH), 7.34 (t, 2H, J = 6.5 Hz, ArH),
.38 (m, 2H, CH ), 4.45 (m, 2H, J = 6 Hz, CH ), 2.50 (s,
H, N=C−CH ), 1.78 (t, 2H, J = 7.5 Hz, CH ), 1.27 (s,
H, J = 7.5 Hz, CH ), 0.88 (t, 3H, CH ). MS (EI):
1
00 mL three-necked flask, and then glacial acetic acid
2
2
(
2 mL) was added dropwise to it. The solution was
3
2
heated to reflux for 2 h, getting lots of solid. The reac-
tion mixture was then filtered taking the advantage of
heat, washed with hot ethanol, and dried to get the title
2
3
m/z (%) = 704 (M+1,12), 703(M, 23), 546 (11), 262 (8),
2
7
9
41 5 2
01 (13), 144 (100). Anal. Calcd for C44H N O : C,
5.09; H, 5.87; N, 9.95. Found: C, 74.92; H, 6.10; N,
.93.
Schiff-base L
1
−L
Naphthalen-2-yloxy)-acetic Acid {1-[9-ethyl-6-(1-{[2-
naphthalen-2-yloxy)-acetyl]-hydrazono}-ethyl)-9H-
9
.
(
(
carbazol-3-yl]-ethylidene}-hydrazide (L1)
was synthesized by the condensation of 2a with 3a.
A pale-yellow solid (0.730 mmol, 73.0 %). m.p
Benzoic Acid {1-[9-ethyl-6-(1-{[2-(phenyl)-formacyl]-
hydrazono}-ethyl)-9H-carbazol-3-yl]- ethylidene}-
L
1
hydrazide (L
4
)
−
1
2
2
1
40−242 °C. IR (KBr):  / cm = 3416, 3055, 2966,
921, 1693, 1629, 1600, 1531, 1467, 1372, 1258, 1122,
065, 1065, 952, 748, 701. 1H NMR (400 MHz,
L
4
was synthesized by the condensation of 2a with 3b.
A pale-yellow solid (0.901 mmol, 90.1 %). m.p
314−315 °C. IR (KBr):  / cm−1 = 3414, 3237, 1638,
1
DMSO-d
5 Hz, ArH), 8.09 (q, 2H, J = 9 Hz, ArH), 7.84 (m, 6H,
ArH), 7.67 (t, 2H, J = 8.5 Hz, ArH), 7.45 (q, 2H, J =
Hz, ArH), 7.34 (m, 6H, ArH), 5.38 (m, 2H, CH ), 4.90
s, 2H, CH ), 4.49 (q, 2H, J = 6 Hz, CH ), 2.49 (s, 6H,
), 1.33 (t,3H, J = 7.5 Hz, CH ). MS (ESI):
6
): δ/ppm = 10.85 (s, 2H, NH), 8.72 (t, 2H, J =
1617, 1528, 1484, 1399, 1284, 1132, 718. H NMR
1
6
(400 MHz, DMSO-d ): δ / ppm = 10.76 (s, 2H, NH),
8.75 (s, 2H, ArH), 8.11 (m, 2H, ArH), 7.92 (s, 4H,
ArH), 7.72 (q, 2H, J = 9 Hz, ArH), 7.59 (q, 2H, J =
9
2
(
2
2
2.5 Hz, ArH), 7.53 (m, 4H, ArH), 4.51 (m, 2H, CH
2.50 (s, 6H, N=C−CH ), 1.35 (t, 3H, J = 2 Hz, CH
2
),
).
N=C−CH
3
3
3
3
m / z (%) = 1373 (2M+Na+, 100), 1174 (22), 770 (25),
MS (EI): m / z (%) = 516 (M+1, 14), 515 (M, 43), 397
(33), 292 (24), 250 (24), 105 (100). Anal. Calcd for
+
6
98 (M+Na , 46), 235 (27). Anal. Calcd for
Croat. Chem. Acta 88 (2015) 1.

4
L. Wu et al., Carbazolyl Diacylhydrazone Schiff-bases
C
32
H
29
N
5
O
2
: C, 74.54; H, 5.67; N, 13.58. Found:
4-Nitro-benzoic Acid {1-[9-ethyl-6-(1-{[2-(4-
C, 74.18; H, 5.65; N, 13.26.
nitrophenyl)-formacyl]-hydrazono}-ethyl)-9H-carbazol-
3
L
-yl]-ethylidene}-hydrazide (L
8
)
Benzoic Acid {1-[9-butyl-6-(1-{[2-(phenyl)-formacyl]-
hydrazono}-ethyl)-9H-carbazol-3-yl] - ethylidene}-
8
was synthesized by the condensation of 2a with 3d.
A orange-yellow solid (0.907 mmol, 90.7 %). m.p
3
hydrazide (L
was synthesized by the condensation of 2c with 3b.
A pale-yellow solid (0.923 mmol, 92.3 %). m.p
5
)
12−313 °C. IR (KBr):  / cm−1 = 3479, 3413, 3231,
638, 1617, 1520, 1487, 1400, 1345, 1277, 1133, 860.
L
5
1
1
6
H NMR (400 MHz, DMSO-d ): δ/ppm = 11.10 (s, 2H,
−
1
2
1
62−263 °C. IR (KBr):  / cm = 3421, 3134, 1637,
NH), 8.83 (s, 2H, ArH), 8.38 (d, 6H, J = 9 Hz, ArH),
.16 (d, 2H, J = 10.5 Hz, ArH), 7.72 (d, 2H, J = 9.5 Hz,
ArH), 7.60 (m, 2H, ArH), 4.53 (m, 2H, CH ), 2.51 (s,
H, N=C−CH ), 1.36 (t, 3H, J = 6 Hz, CH ). MS (EI):
m/z (%) = 606 (M+1, 3), 605 (M, 6), 263 (14), 166 (42),
50 (100), 120 (76), 92 (46). Anal. Calcd for
: C, 63.46; H, 4.49; N, 16.19. Found: C,
3.71; H, 4.88; N, 15.86.
1
606, 1523, 1485, 1399 , 1284, 1132, 720. H NMR
8
(
6
400 MHz, DMSO-d ): δ / ppm = 10.77 (s, 2H, NH),
2
8
5
7
2
0
5
.74 (s, 2H, ArH), 8.11 (m, 2H, ArH), 7.91 (d, 4H, J =
.5 Hz, ArH), 7.69 (m, 2H, ArH), 7.54 (m, 2H, ArH),
6
3
3
.45 (m, 4H, ArH), 4.46 (t, 2H, J = 7 Hz, CH
H, CH ), 2.49 (s, 6H, N=C−CH ), 1.77 (m, 2H, CH
.86 (m, 3H, CH ). MS (EI): m/z (%) = 544 (M+1, 35),
43 (M, 91), 424 (21), 320 (18), 289 (22), 205 (21), 105
: C, 75.11; H, 6.12;
2
), 2.69 (m,
1
2
3
2
),
32 27 7 6
C H N O
3
6
(
100). Anal. Calcd for C34
H
33
N
5
O
2
4-Nitro-benzoic Acid {1-[9-butyl-6-(1-{[2-(4-
N, 12.88. Found: C, 74.79; H, 5.95; N, 13.03.
nitrophenyl)-formacyl]-hydrazono}-ethyl)-9H-carbazol-
3
L
-yl]-ethylidene}-hydrazide (L
9
)
Salicylic Acid {1-[9-ethyl-6-(1-{[2-(2-hydroxyphenyl)-
formacyl]-hydrazono}-ethyl) - 9H-carbazol-3-yl]-
9
was synthesized by the condensation of 2c with 3d.
A yellow solid (0.921 mmol, 92.1 %). m.p 295−296 °C.
ethylidene}-hydrazide (L
was synthesized by the condensation of 2a with 3c.
A pale-yellow solid (0.892 mmol, 89.2 %). m.p
6
)
IR (KBr):  / cm−1 = 3476, 3414, 3237, 2957, 2928,
L
6
2
1
1
8
870, 1639, 1617, 1600, 1526, 1485, 1344, 1285, 1139,
1
6
109, 864. H NMR (400 MHz, DMSO-d ): δ / ppm =
−
1
2
3
1
36−237 °C. IR (KBr):  / cm = 3547, 3477, 3415,
1.10 (s, 2H, NH), 8.78 (s, 2H, ArH), 8.38 (d, 4H, J =
.5 Hz, ArH), 8.18 (d, 4H, J = 9 Hz, ArH), 8.13 (d, 2H,
274, 2966, 2928, 1638, 1618, 1602, 1455, 1562, 1486,
275, 1153, 1099, 748. H NMR (400 MHz DMSO-d
1
6
):
J = 5.5 Hz, ArH), 7.73(t, 2H, J = 9 Hz, ArH), 4.49 (m,
2
2
CH
1
δ/ppm = 11.84 (s, 2H, OH), 11.34 (s, 2H, NH), 8.75 (s,
H, ArH), 8.14 (d, 2H, J = 8.5 Hz, ArH), 8.03 (d, 2H,
J = 8 Hz, ArH), 7.72 (d, 2H, J = 8.5 Hz, ArH), 7.43 (q,
H, CH
H, J = 5.5 Hz, CH
). MS (EI): m/z (%) = 633 (M, 2), 247 (5), 166 (45),
50 (100), 120 (31), 104 (40), 76 (26). Anal. Calcd for
: C, 64.45; H, 4.97; N, 15.47. Found: C,
4.12; H, 5.05; N, 15.08.
2
), 2.51 (t, 6H, J = 2 Hz, N=C−CH
3
), 1.79 (m,
2
2
), 1.32 (m, 2H, CH ), 0.90 (t, 3H,
2
3
2
7
6
H, J = 7 Hz, ArH), 7.03 (m, 4H, ArH), 4.51 (d, 2H, J =
Hz, CH ), 2.50 (s, 6H, N=C−CH ), 1.37 (t, 3H, J =
.5 Hz, CH ). MS (EI): m / z (%) = 548 (M+1, 3), 547
2
3
34 31 7 6
C H N O
6
3
(
M, 7), 426 (9), 152 (18), 121 (100), 92 (44), 65 (26).
Anal. Calcd for C32 : C, 70.19; H, 5.34; N,
2.79. Found: C, 70.40; H, 5.25; N, 12.91.
29 5 4
H N O
1
RESULTS AND DISCUSSION
Salicylic Acid {1-[9-butyl-6-(1-{[2-(2-hydroxyphenyl)-
formacyl]-hydrazono}-ethyl) - 9H- carbazol-3-yl]-
Optimized Synthetic Conditions of the Title Schiff-
bases
ethylidene}-hydrazide (L
was synthesized by the condensation of 2c with 3c.
A pale-yellow solid (0.896 mmol, 89.6 %). m.p
7
)
L
7
The yields of the title carbazolyl diacylhydrazone
Schiff-bases in the condensation reactions between
3,6-diacetyl-9-alkylcarbazole and hydrazide were
found to be highly sensitive to the acid catalyst (glacial
acetic acid) and the reaction time. The synthetic condi-
tions of benzoic acid {1-[9-butyl-6-(1-{[2-(phenyl)-
formacyl]-hydrazono}-ethyl)-9H-carbazol-3-yl]-ethyli-
−
1
2
3
1
57−258 °C. IR (KBr):  / cm = 3547, 3476, 3413,
231, 2962, 2933, 1637, 1617, 1559, 1487, 1455, 1277,
154, 1100, 754. H NMR (400 MHz，DMSO-d
1
6
):
δ/ppm = 11.83 (s, 2H, OH), 11.34 (s, 2H, NH), 8.74 (s,
H, ArH), 8.12 (d, 2H, J = 8.5 Hz, ArH), 8.03 (d, 2H,
J = 6 Hz, ArH), 7.80 (d, 2H, J = 1.5 Hz, ArH), 7.78 (d,
2
dene}-hydrazide (L ) were optimized and expected
5
2
7
6
2
H, J = 1.5 Hz, ArH), 7.71 (d, 2H, J = 8.5 Hz, ArH),
.37 (t, 2H, J = 8.5 Hz, ArH), 4.47(s, 2H, CH ), 2.50 (s,
H, N=C−CH ), 1.81 (q, 2H, J = 7 Hz, CH ), 1.33 (q,
H, J = 7.5 Hz, CH ), 0.89 (t, 3H, J = 7.5 Hz, CH ).
to be helpful to the synthesis of other title Schiff-
bases.
2
3
2
Because the glacial acetic acid can enhance the
electropositivity of the carbonyl carbon, promote the
breakdown of the carbazolyl diacylhydrazone Schiff-
bases, and reduce the nucleophilic ability of the amino,
the condensation reactions were sensitive to the acid
catalyst (glacial acetic acid).
2
3
MS (EI) m / z (%): 576(M+1, 7), 575 (M, 12), 424(17),
19(12), 262 (12), 137(24), 121(100). Anal. Calcd for
: C, 70.94; H, 5.78; N, 12.17. Found: C,
0.76; H, 5.84; N, 12.17.
3
34 33 5 4
C H N O
7
Croat. Chem. Acta 88 (2015) 1.

L. Wu et al., Carbazolyl Diacylhydrazone Schiff-bases
Table 1. The yields of the title Schiff-bases
5
1 9
Table 3. The UV spectra data of the title Schiff-bases L –L
Schiff-base
Yield(a) / %
10.1
Yield(b) / %
73.0
Schiff-base
λ
a,1 / nm
302
317
310
308
290
297
266
268
277
λa,2 / nm
L
1
L
2
L
3
L
4
L
5
L
6
L
7
L
8
L
9
L
1
L
2
L
3
L
4
L
5
L
6
L
7
L
8
L
9
330
348
332
340
320
326
307
310
312
11.4
75.2
12.5
73.5
10.3
90.1
11.8
92.3
13.4
89.2
10.6
89.6
12.9
90.7
10.4
92.1
(
a)
b)
The yields of L
The yields of L
1
–L
9
in the absence of glacial acetic acid.
in glacial acetic acid.
(
1
–L
9
compound L was up to 92.3 % under this reaction
5
condition.
In order to investigate the influence of the acid
catalyst on the yields of the title Schiff-bases, the con-
densation reactions of 3,6-diacetyl-9-alkylcarbazole
with hydrazide were carried out in the presence of gla-
cial acetic acid or not. The experimental data were listed
in Table 1. It is seen from the table 1 that the yields of
the title Schiff-bases were no more than 15 % in the
absence of glacial acetic acid. However, the yields of
Effect of Substituents on the Properties of the Title
Schiff-bases
All the title Schiff-bases showed the luminescence
properties, however, their fluorescent intensities were
quite different. In order to evaluate the relationships
between the luminescence properties and the structures
of the title Schiff-bases, the UV spectra and fluores-
cence emission spectra of the title Schiff-bases were
measured.
L
4
−L
9
were all about 90 % in the presence of glacial
−L may be
acetic acid. The slightly lower yields of L
1
3
due to the steric hindrance of naphthalene-2-yloxy. The
results indicated that the addition of the glacial acetic
acid and the steric hindrance from the substituents in
benzene ring had remarkable influence on the yields of
the title Schiff-bases, and the electronic effect of the
substituents had little influence on them.
In order to optimize the synthetic conditions of the
title Schiff-bases, the influences of the reaction time and
the volumn fraction of glacial acetic acid on the yield of
The UV spectra data of the title Schiff-bases (L
) were listed in Table 3 and the UV spectra were
shown in Figure 1 and Figure 2. The UV absorption
bands of L –L appeared at λ and λ were assigned
1
–
L
9
1
9
a
,
1
a 2
,
to the л–π* and n–π* transition respectively.
The fluorescence emission spectra of the title
Schiff-bases (L
1
–L ) were excitated by their respective
9
maximum UV absorption peak wavelengths.
The fluorescence emission spectra of the com-
L
5
were investigated. The experimental data were listed
in Table 2.
Based on the optimization experimental data in
Table 2, it was concluded that the optimal synthesis
conditions of the compound L via the condensation of
pounds L
the fluorescence emission intensities of the compounds
and L were strong due to the introduction of naph-
thalene-2-yloxy which could improve the structural
planarity and conjugation effect of the compounds L
and L . However, when a butyl group was bonded to the
carbazole ring, such as the compound L , the fluores-
cence emission intensity was observed to be much
weaker relative to that of the compounds L and L
1
–L
3
were shown in Figure 3. It was found that
L
1
2
5
1
benzoylhydrazine with 3, 6-diacetyl-9- butylcarbazole
were that the volumn fraction of glacial acetic acid was
2
3
2
0 % and the reaction time was 2 h, the yield of the
Table 2. The yields of the Schiff-base L
5
1
2
because the increase of alkyl carbon numbers in the
carbazole ring resulted in the reduction of the planarity
of the whole molecular structure. In addition, the title
Schiff-bases with benzene ring, such as the compounds
vol.(a) / %
Yield/ %
Entry
t / h
1
1
2
3
4
5
6
0
0
3
1
45.1
74.5
85.6
92.3
92.3
L
4
–L , showed particularly weak fluorescence because
9
10
10
20
30
1
of their poor conjugated structure. The experimental
results clearly indicated that both the naphthalene-2-
yloxy structure and the change of the alkyl group in the
carbazole ring had remarkable influence on the lumi-
nescence properties of the title Schiff-bases.
2
2
2
(a)
The volume fraction of glacial acetic acid.
Croat. Chem. Acta 88 (2015) 1.

6
L. Wu et al., Carbazolyl Diacylhydrazone Schiff-bases
CONCLUSION
In conclusion, an efficient synthetic approach to nine
novel carbazolyl diacylhydrazone Schiff-bases obtained
from carbazole and hydrazide by alkylation and Friedel-
Crafts acylation have been developed. All synthesized
1
compounds were examined by H NMR, MS, IR, ele-
mental analysis and so on. The yield of the title Schiff-
bases rise up to 92.3 % under the optimized synthetic
conditions that the volumn fraction of glacial acetic acid
was 20 % and the reaction time was 2 h. The relation-
ship between luminescence properties and the structures
of the title Schiff-bases were studied by introducing
naphthalene-2-yloxy, benzene ring and alkyl. It was
observed that the introduction of naphthalene-2-yloxy
causes the fluorescence emission intensity of the title
Schiff-bases to be increased considerably. But the elec-
tronic effects of benzene ring and the substituents in
benzene ring barely affect the luminous intensity of the
title Schiff-bases.
1 3
Figure 1. UV spectra of the Schiff-bases (L –L ).
Acknowledgements. The authors are grateful for the financial
support of the National Natural Science Foundation of China
(No. J1103312, No.21341010), the Innovative Research Team
in University (No.IRT1238) as well as the Science and Tech-
nology Project of Hunan provincial Science and Technology
Department (No.2012GK3156). We also thank Dr. William
Hickey, the U.S. professor of HRM, for the English editing on
this paper.
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