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1.
Johan Alauzun Ahmad Mehdi Rola Mouawia Catherine Reyé Robert J. P. Corriu 《Journal of Sol-Gel Science and Technology》2008,46(3):383-392
We report the preparation of a new class of lamellar hybrid organic–inorganic materials obtained by self-assembly of bridged
organosilica precursors containing long alkylene chains during the sol–gel process. The self-assembly is induced by lipophilic
van der Waals interactions. The introduction of –SS– bonds in the core of the alkylene chains permitted the functionalisation
of lamellar materials, which were subsequently transformed into SH and –SO3H groups. This methodology was extended to the formation of lamellar hybrid materials containing amino groups thanks to CO2 as bridging groups as well as the formation of lamellar hybrid materials containing carboxylic groups. In this last case,
the hydrolysis and polycondensation of cyanoalkyltrialkoxysilanes permitted the one pot synthesis of lamellar hybrid materials
thanks to in situ hydrogen bonds formation between carboxylic acids groups. All these functional lamellar materials exhibit
a very high chelating capability towards transition metal and lanthanide ions. 相似文献
2.
A Macrocyclic Fluorophore Dimer with Flexible Linkers: Bright Excimer Emission with a Long Fluorescence Lifetime
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Hiroshi Osaki Dr. Chih‐Ming Chou Prof. Dr. Masayasu Taki Dr. Kai Welke Prof. Dr. Daisuke Yokogawa Prof. Dr. Stephan Irle Prof. Dr. Yoshikatsu Sato Prof. Dr. Tetsuya Higashiyama Dr. Shohei Saito Prof. Dr. Aiko Fukazawa Prof. Dr. Shigehiro Yamaguchi 《Angewandte Chemie (International ed. in English)》2016,55(25):7131-7135
Bright fluorescent molecules with long fluorescence lifetimes are important for the development of lifetime‐based fluorescence imaging techniques. Herein, a molecular design is described for simultaneously attaining long fluorescence lifetime (τ) and high brightness (ΦF×?) in a system that features macrocyclic dimerization of fluorescent π‐conjugated skeletons with flexible linkers. An alkylene‐linked macrocyclic dimer of bis(thienylethynyl)anthracene was found to show excimer emission with a long fluorescence lifetime (τ≈19 ns) in solution, while maintaining high brightness. A comparison with various relevant derivatives revealed that the macrocyclic structure and the length of the alkylene chains play crucial roles in attaining these properties. In vitro time‐gated imaging experiments were conducted as a proof‐of‐principle for the superiority of this macrocyclic fluorophore relative to the commercial fluorescent dye Alexa Fluor 488. 相似文献
3.
为了理解gemini表面活性剂柔性烷基联接链在自组织过程中的特殊作用,我们合成了三种gemini表面活性剂烷基-a,w-二(二-十二烷基甲基溴化铵)(记为2C12-s-2C12×2Br (s=3, 6, 8))。2C12-s-2C12×2Br在水表面构成铺展膜后,由于每个分子带有4根烷烃链,它们形成了稠密的烷烃尾链层。增强的烷烃尾链与联接链间的疏水相互作用促使联接链弯曲朝向空气一端,可发生弯曲的联接链长度要小于吸附在水溶液表面上的gemini表面活性剂C12-s-C12×2Br,后者每个分子只有2根烷烃链。由此可见,增强的烷烃尾链与联接链间的疏水相互作用可以有效地促进联接链的弯曲。 相似文献
4.
Lui Niimi Shuichi Hiraoka Tsutomu Yokozawa 《Journal of polymer science. Part A, Polymer chemistry》2005,43(22):5440-5448
Polyethers with propargyl side chains were synthesized by the acid‐catalyzed reaction of dialdehydes 1 , alkylene bis(trimethylsilyl) ethers 2 , and allenyltrimethylsilane 4 . When ethylene glycol bis(trimethylsilyl) ether was used as 2 , only oligomer was obtained. However, the use of 2 with longer carbon chains gave the desired polyethers consisting of 1 , 2 , and 4 in the molar ratio 1:1:2 in good yields in the presence of 10 mol % triphenylmethyl perchlorate (TrClO4) at ?20 °C. This polyether was treated with organometallic reagents such as Co complex or CuCl to give a cross‐linked polymer. This polymer synthesis is unusual in that it concurrently constructs both the polymer backbone and the functional side chains from three starting compounds. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5440–5448, 2005 相似文献
5.
Stanislaw Penczek Julia Pretula Krzysztof Kaluzynski 《Journal of polymer science. Part A, Polymer chemistry》2005,43(3):650-657
Triblock copolymer poly(ethylene glycol)‐poly(alkylene phosphate)‐poly(ethylene glycol) was prepared by first reacting hexamethylene glycol with dimethyl‐H‐phosphonate at conditions of transesterification and then replacing the CH3OP(O)(H)O‐… end‐groups by monomethyl ether of poly(ethylene glycol). The course of reaction was studied by 31P NMR indicating complete conversion. After oxidation the poly(alkylene H‐phosphonate was converted into the final triblock polyphosphate. This triblock copolymer was used as a modifier of CaCO3 crystallization. Unusual semi open empty spheres resulted, composed of small crystallites of the size (diameter) equal to 40–90 nm. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 650–657, 2005 相似文献
6.
Akira Matsumoto Tomonori Ohashi Hiroaki Oe Hiroyuki Aota Jun‐Ichi Ikeda 《Journal of polymer science. Part A, Polymer chemistry》2000,38(24):4396-4402
As an extension of our work on the elucidation of the mechanism and control of 3‐dimensional network formation in the free‐radical crosslinking polymerization and copolymerization of multivinyl compounds with the aim to molecularly design vinyl‐type network polymers, novel amphiphilic polymers were prepared as crosslinked polymer precursors. Thus, benzyl methacrylate, a nonpolar monomer, was copolymerized radically with 5 mol % of triicosaethylene glycol dimethacrylate [CH2C(CH3)CO(OCH2CH2)23OCOC(CH3)CH2], a polar monomer, in the presence of lauryl mercaptan as a chain transfer agent. The resulting prepolymers (i.e., vinyl‐type network‐polymer precursors or amphiphilic polymers) were characterized mainly by viscometry using t‐butylbenzene (t‐BB) and a t‐BB/MeOH (80/20) mixture as solvents. The viscosities in the t‐BB/MeOH (80/20) mixture were quite high compared with those in t‐BB, and completely reversed concentration dependencies were observed in the solvents. These are discussed by considering the difference in conformation and the shrinkage of polar, flexible polyoxyethylene units or the entanglement of nonpolar, rigid primary chains. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 4396–4402, 2000 相似文献
7.
Yuji Suzaki Yusuke Yoshigoe Kohtaro Osakada 《Journal of polymer science. Part A, Polymer chemistry》2013,51(17):3627-3635
Oligo‐ and poly(ferrocenylene alkylene)s, [Fe(C5H5‐x)(C5H5‐y)CHR]n (x = y = 1 or x = 2, y = 0; R = alkyl, aryl), were synthesized by Lewis acid‐promoted addition‐condensation polymerization of ferrocene with aldehydes. The reaction of alkyl aldehydes, such as n‐hept‐CHO, EtCHO and nBuCHO, with ferrocene yields a mixture of the cyclic and linear poly(ferrocenylene alkylene)s, while aryl aldehyde, such as C6F5CHO, CF3C6H4‐4‐CHO and MeC6H4‐4‐CHO, forms the linear polymers exclusively. The linear polymer has terminal ? Fe(C5H4)(C5H5) and ? CH2Aryl groups, which are characterized by high resolution mass spectroscopy. Results of addition‐condensation polymerization of ferrocenemethanol catalyzed by BF3 indicate that the propagating polymer of the above addition‐condensation polymerization contains terminal 1‐hydroxyalkyl‐ferrocenylene group, ? Fe(C5H4)[C5H4{CH(OH)R}]. The trimer prepared from ferrocene and paraformaldehyde dimethylacetal contains 1,1′‐, 1,2‐, and 1,3‐ferrocenylene units, suggesting that the polymers obtained from alkyl and aryl aldehydes are also composed of these structural units. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 3627–3635 相似文献
8.
Thierry Thami Gihane Nasr Hanan Bestal Arie Van Der Lee Bruno Bresson 《Journal of polymer science. Part A, Polymer chemistry》2008,46(11):3546-3562
Thin films of crosslinked polymethylhydrosiloxane (PMHS) have been grafted on silica using the sol–gel process allowing further functionalization by effective quantitative hydrosilylation of SiH groups by olefins within the network. Postfunctionalization gives the polysiloxane network with n‐alkyl side chains. The PMHS coating was prepared by room temperature polycondensation of a mixture of methyldiethoxysilane HSiMe(OEt)2 monomer and triethoxysilane HSi(OEt)3 (TH) as crosslinker. The surface‐attached films are chemically stable and covalently bonded to the silica surface. Subsequently, films were functionalized without delamination. We showed by FTIR spectroscopy how the crosslinking ratio and the molecular size of the alkenes precursors influence the extent of the hydrosilylation reaction of SiH groups in the PMHS network. We have determined that quasi‐full olefin addition catalyzed by a platinum complex occurred within soft networks of less than 5% TH with 1‐alkenes CH2?CH(CH2)n‐2CH3 of various alkyl chain lengths (n = 5, 11, 17). Powders of PMHS gel were also modified with 1‐alkenes by hydrosilylation. The SiH groups within the soft gel (5% crosslinked) were fully functionalized as shown by 29Si and 1H solid‐state NMR. The structure of functionalized polysiloxane with n‐octadecyl and n‐dodecyl side chains was studied by FTIR, wide angle X‐ray diffraction, and DSC showing crystallization of the long n‐alkyl chains in the network. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 3546–3562, 2008 相似文献
9.
Gisèle Volet Anne‐Cécile Lasne Deschamps Catherine Amiel 《Journal of polymer science. Part A, Polymer chemistry》2010,48(11):2477-2485
The α,ω‐end‐capped poly(2‐methyl‐2‐oxazoline) (Cn‐POXZ‐Cn) have been synthesized by a one‐pot process using cationic ring‐opening polymerization with an appropriate initiator and terminating agent. The polymers bearing different alkyl groups C12 and C18 have molecular weight in the range of 2.4 × 103 to 14 × 103 with a small polydispersity index. The solution behavior of the free chains has been analyzed in a nonselective solvent, dichloromethane, by small‐angle neutron scattering and dynamic light scattering. These amphiphilic polymers associate in water to form flower‐like micellar structures. Critical micelle concentrations, investigated by fluorescence technique, are in the range of 0.03–0.5 g L?1 and are dependent on the hydrophilic/lipophilic balance. The structural properties of the aggregates have also been investigated by viscometry. Intrinsic viscosities of these polymers are in the same range as that of the precursors poly(2‐methyl‐2‐oxazoline) (POXZ) and mono‐functionalized polymers. Large viscosity increase corresponding to intermicellar bridging was observed in the vicinity of the micelle overlap concentration. Addition of hydroxypropyl β‐cyclodextrin (HβCD) has dissociated the aggregates and the intrinsic viscosities of the HβCD‐end‐capped chains have become comparable with the ones of POXZ precursor chains. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 2477–2485, 2010 相似文献
10.
A simple route to ω-aminoalkyltriethoxysilanes with variable alkylene chain lengths, (EtO)3Si(CH2)nNH2 (n = 5, 11) is described. These silyl linkers have been used to prepare urea-based compounds with H-bonding and hydrophobic interactions which enable the self-assembly of the molecules. These molecular precursors are suitable for the obtention of nano-structured hybrid silicas. 相似文献
11.
Synthesis of Long,Palladium End‐Capped Polyynes through the Use of Asymmetric 1‐Iodopolyynes
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Dr. Bartłomiej Pigulski Dr. Nurbey Gulia Dr. Sławomir Szafert 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(49):17769-17778
The synthesis of a unique series of long, asymmetric 1‐iodopolyynes ( 1 ‐CnI and 2 ‐CnI) with the sp‐hybridized carbon chain up to a decapentayne is reported. These compounds were then used as substrates in reactions with Pd(PPh3)4 leading to another series of palladium end‐capped polyynes, which were unstable in solution. Organometallic octatetraynes 1 ‐C8[Pd]I, 2 ‐C8[Pd]I, and decapentayne 1 ‐C10[Pd]I are palladium end‐capped polyyne compounds with the longest carbon chains reported so far. All the complexes as well as their organic precursors were fully characterized by NMR, HRMS(ESI), IR, TGA‐DTA, and UV/Vis techniques, and the X‐ray crystal structures of two silyl‐protected precursors and one palladium complex are presented. The synthetic approach for palladium species is envisioned as a general route for the synthesis of labile organometallic polyynes. 相似文献
12.
Veronica Marin Elisabeth Holder Ulrich S. Schubert 《Journal of polymer science. Part A, Polymer chemistry》2004,42(2):374-385
Methyl methacrylate‐containing bipyridine monomers were synthesized with a hydoxy‐functionalized bipyridine. The 4′‐methyl group of the 2,2′‐bipyridine was used to introduce hydoxy‐functionalized alkyl spacers of two different lengths. Two, different synthetic routes were applied for the preparation of the hydoxy‐functionalized bipyridine via a bromo‐(C7 spacer) or a silylated‐(C3 spacer) intermediate. A copolymer of poly(methyl methacrylate) with bipyridine units in the side chains was prepared by free‐radical copolymerization and characterized with 1H NMR, ultraviolet–visible, and IR spectroscopy as well as gel permeation chromatography. The bipyridine units of the copolymer were reacted with ruthenium bipyridine precursors. The resulting graft copolymers displayed promising photophysical and electrochemical properties, opening interesting perspectives for applications in the field of solar‐cell devices. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 374–385, 2004 相似文献
13.
Ryota Seto Takashi Sato Takahiro Kojima Katsumoto Hosokawa Yasuhito Koyama Gen‐Ichi Konishi Toshikazu Takata 《Journal of polymer science. Part A, Polymer chemistry》2010,48(16):3658-3667
Syntheses of 2,2′‐bisalcoholic group‐substituted 9,9′‐spirobifluorene monomers 2 were performed by the reaction of 2,2′‐dihydroxy‐9,9′‐spirobifluorene 2a with haloalcohols. Polycarbonates consisting of 9,9′‐spirobifluorene skeleton in the main chain (PC 4 ) were synthesized by the polycondensation of 2,2′‐bisalcoholic monomers 2 and triphosgene or diphenyl carbonate. PC 4 showed good thermal stability: the 5% weight loss temperature was over 330 °C under both nitrogen and air atmospheres. The glass transition temperature was in a range of 16–269 °C estimated by differential scanning calorimetry, depending on the flexibility of the alkylene or oxyethylene chains of 2 . PC 4 showed high solubility toward ordinary organic solvents such as CHCl3, benzene, and THF, making possible the preparation of the flexible thin films. Very high refractive index in a range of 1.62–1.66 at 589 nm was observed although PC 4 consists only of C, H, and O atoms, whereas very low degree of birefringence was confirmed. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3658–3667, 2010 相似文献
14.
Synthesis of maltopentaose‐conjugated surface‐active styrenic monomers and their micellar homopolymerization in water
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Daichi Togashi Issei Otsuka Redouane Borsali Atsushi Narumi Seigou Kawaguchi 《Journal of polymer science. Part A, Polymer chemistry》2015,53(14):1671-1679
Maltopentaose (Mal5)‐conjugated surface‐active styrenic monomers 1a , 1b , and 1c are described, which contain hydrophobic spacers, such as C1, C5, and C7 alkylene chains, respectively. The glycomonomers 1a‐c were synthesized by the direct β‐N‐glycosyl reaction of styrene derivatives with aminoalkyl groups 4a‐c onto Mal5 in dry methanol, followed by the N‐acetylation with acetic anhydride. The self‐assembling properties for the aqueous solutions of 1a‐c were characterized by surface tension measurements and light scattering experiments, providing the physicochemical parameters for the formed 1a‐c micelles including the critical micelle concentration, apparent hydrodynamic radius (Rh,app), and weight average aggregation number (Nagg). The transmission electron microscope observations revealed the most important result in this study that 1a produced loose spherical micelles with the number average diameter (dn) of 26 nm, while both 1b and 1c formed worm‐like micelles with the polymerizable core and the Mal5 shell, whose number average contour lengths (lns) were 130 nm and 68 nm, respectively. The radical homopolymerizations of 1a‐c in water provided a substantial result in this study that 1b and 1c , that is, the glycomonomers forming the worm‐like micelles, showed a very high homopolymerizability in water. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 1671–1679 相似文献
15.
Paul G. Jene James A. Ibers 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(6):705-707
The crystal structures of two elaborated‐porphyrin precursors have been determined. In the crystalline state, 2‐(1,3‐dithian‐2‐yl)benzaldehyde, C11H12OS2, has its dithiane ring in a slightly distorted chair conformation. The molecules pack in anti‐parallel chains. N‐{2‐[2‐(1,3‐Dioxan‐2‐yl)phenoxy]ethyl}phthalimide, C20H19NO5, is in a folded conformation. The dihedral angle between the phthalimide and phenyl planes is 80.07 (3)°. In the crystalline states, molecules stack on top of one another. 相似文献
16.
Jordan O. Lerach Brian D. Leskiw 《Rapid communications in mass spectrometry : RCM》2008,22(24):4139-4146
Gas‐phase ligand exchange reactions between M(acac)2 and M(hfac)2 species, where M is Cu(II) and/or Ni(II), were observed to occur in a double‐focusing reverse‐geometry magnetic sector mass spectrometer. The gas‐phase mixed ligand product, [M(acac)(hfac)]+, was formed following the co‐sublimation of either homo‐metal or hetero‐metal precursors. The gas‐phase formation of [Cu(acac)(hfac)]+ from hetero‐metal precursors is reported herein for the first time. The [Ni(acac)(hfac)]+ complex is also observed for the first time to form following the co‐sublimation of not only Ni precursors, but also from separate Ni and Cu precursors. The corresponding fragmentation patterns of these species are also presented, and the mixed metal mixed ligand product [NiCu(acac)2(hfac)]+ is observed. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
17.
Guowei Wang Bin Hu Xiaoshan Fan Yannan Zhang Junlian Huang 《Journal of polymer science. Part A, Polymer chemistry》2012,50(11):2227-2235
The tadpole‐shaped copolymers polystyrene (PS)‐b‐[cyclic poly(ethylene oxide) (PEO)] [PS‐b‐(c‐PEO)] contained linear tail chains of PS and cyclic head chains of PEO were synthesized by combination of Glaser coupling with living anionic polymerization (LAP) and ring‐opening polymerization (ROP). First, the functionalized polystyrene‐glycerol (PS‐Gly) with two active hydroxyl groups at ω end was synthesized by LAP of St and the subsequent capping with 1‐ethoxyethyl glycidyl ether and then deprotection of protected hydroxyl group in acid condition. Then, using PS‐Gly as macroinitiator, the ROP of EO was performed using diphenylmethylpotassium as cocatalyst for AB2 star‐shaped copolymers PS‐b‐(PEO‐OH)2, and the alkyne group was introduced onto PEO arm end for PS‐b‐(PEO‐Alkyne)2. Finally, the intramolecular cyclization was performed by Glaser coupling reaction in pyridine/Cu(I)Br/N,N,N′,N″,N″‐pentamethyldiethylenetriamine system under room temperature, and tadpole‐shaped PS‐b‐(c‐PEO) was formed. The target copolymers and their intermediates were well characterized by size‐exclusion chromatography, proton nuclear magnetic resonance spectroscopy, and fourier transform infrared spectroscopy in details. The thermal properties was also determined and compared to investigate the influence of architecture on properties. The results showed that tadpole‐shaped copolymers had lower Tm, Tc, and Xc than that of their precursors of AB2 star‐shaped copolymers. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
18.
Eli Ruckenstein Hongmin Zhang 《Journal of polymer science. Part A, Polymer chemistry》2000,38(8):1195-1202
A successive method for preparing novel amphiphilic graft copolymers with a hydrophilic backbone and hydrophobic side chains was developed. An anionic copolymerization of two bifunctional monomers, namely, allyl methacrylate (AMA) and a small amount of glycidyl methacrylate (GMA), was carried out in tetrahydrofuran (THF) with 1,1‐diphenylhexyllithium (DPHL) as the initiator in the presence of LiCl ([LiCl]/[DPHL]0 = 2), at −50 °C. The copolymer poly(AMA‐co‐GMA) thus obtained possessed a controlled molecular weight and a narrow molecular weight distribution (Mw /Mn = 1.08–1.17). Without termination and polymer separation, a coupling reaction between the epoxy groups of this copolymer and anionic living polystyrene [poly(St)] at −40 °C generated a graft copolymer with a poly(AMA‐co‐GMA) backbone and poly(St) side chains. This graft copolymer was free of its precursors, and its molecular weight as well as its composition could be well controlled. To the completed coupling reaction solution, a THF solution of 9‐borabicyclo[3.3.1]nonane was added, and this was followed by the addition of sodium hydroxide and hydrogen peroxide. This hydroboration changed the AMA units of the backbone to 3‐hydroxypropyl methacrylate, and an amphiphilic graft copolymer with a hydrophilic poly(3‐hydroxypropyl methacrylate) backbone and hydrophobic poly(St) side chains was obtained. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 1195–1202, 2000 相似文献
19.
Methods of preparation of novel composites of poly(ϵ‐caprolactone) and a modified Mg/Al hydrotalcite
Loredana Tammaro Mariarosaria Tortora Vittoria Vittoria Umberto Costantino Fabio Marmottini 《Journal of polymer science. Part A, Polymer chemistry》2005,43(11):2281-2290
12‐Hydroxydodecanoate (HD) anions were intercalated, via an ion‐exchange procedure, onto a Mg/Al hydrotalcite‐like compound with the formula [Mg0.65Al0.35(OH)2](NO3)0.35·0.56H2O. The obtained intercalate, characterized by chemical and thermal analyses, X‐ray powder diffraction, and Fourier transform infrared spectroscopy, had the formula [Mg0.65Al0.35(OH)2](NO3)0.08(HD)0.28·0.56H2O and an interlayer distance of 2.27 nm. Structural considerations indicated that the charge‐balancing HO? (CH2)11? COO? anions were accommodated in the interlayer region as a monofilm of partially interdigitated alkyl chains in a trans planar conformation and bearing the alcoholic group. The organically modified hydrotalcite was used to prepare novel composites based on poly(?‐caprolactone) (PCL) with different procedures: (1) solvent casting, (2) ring‐opening polymerization of ?‐caprolactone, and (3) blending of precursors consisting of a PCL intercalated oligomer with a high‐molecular‐weight PCL. Microcomposites were obtained by the solvent casting of a mixture of a high‐molecular‐weight PCL and the modified hydrotalcite. The ring‐opening polymerization of ?‐caprolactone initiated by the ? OH groups of the alkyl chains intercalated in the hydrotalcite led to hybrid materials in which a low‐molecular‐weight PCL was in part intercalated into the modified hydrotalcite. Nanocomposites containing exfoliated hydrotalcite were obtained through the mixing, in different weight ratios, of hybrids consisting of PCL oligomers and modified hydrotalcite with a commercial high‐molecular‐weight PCL. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 2281–2290, 2005 相似文献
20.
Anita M. Grzekiewicz Agata Ostrowska Maciej Kubicki 《Acta Crystallographica. Section C, Structural Chemistry》2020,76(3):250-257
The crystal structures of 6‐aminothiocytosine (systematic name: 4,6‐diamino‐1,2‐dihydropyrimidine‐2‐thione, DAPMT, C4H6N4S), its hemihydrate (0.5H2O) and its dimethylformamide (DMF, C3H7NO) monosolvate were compared, and the influence of the type of solvent on the supramolecular motifs was analysed. In all three crystal structures, there are two symmetry‐independent molecules (A and B), and these molecules are connected by three relatively short and directional hydrogen bonds to form chains of alternating A and B molecules. A further organization of these chains is dependent on the nature of the solvent molecule. In the unsolvated form, two orientations of the neighbouring chains are observed, and similar motifs – but only one per structure – can be observed in the solvated structures. These two different motifs can be connected by two different kinds of contacts, i.e. either π–π (hemihydrate) or staple‐supported S…S (DMF). In the crystal structures, the O atoms of the solvent molecules are double acceptors of the same type of hydrogen bonds and bind the chains of DAPMT molecules into different motifs (dimeric or infinite chains). A Hirshfeld fingerprint analysis was used for visualization and additional interpretation of these results. 相似文献