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1 , and N(Tf)(2) = bis(trifluoromethylsulfonyl)imide).
2 d carbonylation and ring closure to form the imide.
3 chlorin-isoimide in addition to the chlorin-imide.
4 a hydrogen storage mechanism for the ternary imide.
5 mpact on the hydrogenation properties of the imide.
6 ment of regioselectively reduced N-homoallyl imides.
7 aldehydes, ketones, esters, carbamates, and imides.
8 possibility to successfully ionize PAHs and imides.
9 of the bis(imino)pyridine alkyl-substituted imides.
10 e efficient access to a variety of hydrazino imides.
11 alcohols to afford the corresponding bis-SES imides.
13 H by 1 to give R(*), which may add to either imide 1 or amide 2, each featuring significant N-based r
14 magnetically coupled to an imidyl radical (S(imide) = 1/2) and a closed-shell, dianionic bis(imino)py
16 ether adduct of an asymmetric niobium(V) bis(imide) 2.OEt2 containing the monoazabutadiene (MAD) liga
17 c(Me){NHB(NAr'CH)2} (18) generated transient imide 25 via rate-determining, first-order methane elimi
18 ,N'-4,4'-biphenylene(bis(triphenyl)phosphine imide) (3) forms radical cationic and a dicationic speci
19 M a trans 2-octenoylated, citrate-containing imide 6 was nearly 5-fold more effective in stimulating
20 nusual complexes including the ruthenium(IV) imide, 7-OMe, as well as the Ru(II) azide adduct 8-OMe.
23 ne product or reversibly form an aziridinium imide (AI) intermediate that does not participate in the
24 ononitrile are much more stable than lithium imides, alane binding dramatically reduces the enamide p
25 formation of the bis(imino)pyridine vanadium imide amide compounds, ((iPr)BPDI)V(NHAr)NAr, were obser
27 rin a, 13(1)/15(1)-N-alkyl isoimide, and the imide analogues were found to be more stable with a sign
28 thylimidazolium bis(trifluoromethanesulfonyl)imide and 1-butyl-3-methylimidazolium bis(trifluorometha
30 is of new organic materials based on arylene imide and bis(imide) dyes, such as perylene-3,4:9,10-bis
31 ng by a regioselective reduction of a chiral imide and cyclization with trifluoromethanesulfonic acid
32 xyuridine without the protection at the N(3)-imide and provides a facile and general access to versat
38 oxyethane, TFSI=bis(trifluoromethanesulfonyl)imide) and realize the best cycling stability among all
39 pected bicyclo[3.2.1]octane (tropane) ether, imide, and amine derivatives but also to unexpected bicy
40 e performed on model compounds of the amide, imide, and cyclic 1,2- and 1,3-species to better underst
41 e utility of this method to generate amides, imides, and carbamates is illustrated by a one-pot synth
42 both aryl- and alkyl-substituted nickel(III)-imides, and examples of both types have been isolated an
44 alently attached to a 4-aminonaphthalene-1,8-imide (ANI) chromophore and a naphthalene-1,8:4,5-bis(di
45 s found that the bis(trifluoromethylsulfonyl)imide anion has the greatest affinity for CO2, while the
47 growth process afforded surface-bound oligo-imide architectures composed of alternating components w
48 (14,15)N ENDOR measurements of the bridging imide are consistent with an allyl radical molecular orb
51 Reactions involving the olefinic bond of the imide as well as its carbonyl groups are observed and an
52 he discovery of tert-leucinol derived cyclic imides as a potent series of novel P3 capping groups.
53 e was obtained, whereas the use of amines or imides as nucleophile afforded a mixture of the two stru
56 he protection of the NH group of a series of imides, azinones (including AZT), inosines, and cyclic s
57 olymers and poly(tert-butyl ester norbornene imide-b-N-methyloxanorbornene imide) copolymers were pre
58 thylimidazolium bis(trifluoromethanesulfonyl)imide, background subtraction is necessary at a macrodis
59 provides a facile entry into a new class of imide-based "3 + 3" macrocyclic trimer (trezimide), toge
61 Although it shares a binding site with other imide-based natural product translation inhibitors, CL e
62 nolates to alpha,beta-unsaturated esters and imides bearing adjacent stereocenters (X, Y = H, Me, OR)
65 for barbiturate extraction over other cyclic imides becomes better in the presence of barbiturate rec
66 hylimidazolium bis(trifluoromethanesulfonyl)-imide, BMI(Tf2N), has been developed and characterized f
67 ethylimidazolium bis(trifluoromethylsulfonyl)imide (BMIm-TFSI), and some combination of ferrocene (Fc
68 ethylimidazolium bis(trifluoromethylsulfonyl)imide (BmimNTf2) were investigated with two-dimensional
70 ylpyrrolidinium-bis(trifluoromethanesulfonyl)imide (BMP-TFSI) IL is beneficial for glucose detection,
72 omerization about a highly conserved Trp-Pro imide bond in a region of the TAD that is required for n
76 planar compounds with relatively short Fe-N(imide) bond lengths and two-electron reduction of the re
78 of restricted rotation around that C(aryl)-N(imide) bond, which locks the carboxylic acid recognition
81 olium)dodecane bis[(trifluoromethyl)sulfonyl]imide bromotrichloroferrate(III) ([(C16BnIM)2C12(2+)][NT
83 tion for the desymmetrization of meso-cyclic imides by hydrogenation with 8-K are also described here
84 pentadienyl) titanium amides, hydrazides and imides by proton coupled electron transfer (PCET) is des
85 avoring one rotamer of the resulting Ni(III)-imide, by locking the phenyl ring in a perpendicular ori
86 resulting from restricted rotation about the imide C-N bond; the 13C NMR spectra and stereochemistry
87 low coverages, ordered overlayers of phenyl imide (C(6)H(5)N) form at saturation coverage, indicatin
90 ethylimidazolium bis(trifluoromethylsulfonyl)imide ([C2mim][NTf2]) and N-butyl-N-methyl-pyrrolidinium
91 ethylimidazolium bis(trifluoromethylsulfonyl)imide ([C2mim][NTf2]) is demonstrated using low-cost pla
93 hylimidazolium bis[(trifluoromethyl)sulfonyl]imide (C4mim+Tf2N(-)), rather than the hydrated, neutral
94 thylimidazolium bis(trifluoromethanesulfonyl)imide ([C4mim][NTf2]) using a surface forces apparatus w
95 4mim][OTf]), and bis(trifluoromethylsulfonyl)imide ([C4mim][Tf2N]) were synthesized via a halide-free
96 butylimidazolium bis(trifluoromethylsulfonyl)imide ([C4MIM][TFSI]) were confined within the hybrid ne
97 thylimidazolium bis(trifluoromethanesulfonyl)imide [C4mim][NTf2], with concentration varied using met
100 thylimidazolium bis(trifluoromethylsulfonyl)-imide [C6MIM][Tf2N] as ionic liquid for the detection of
102 ese macrocyclic inhibitors identified a P(3) imide capped analogue 52 that was 20 times more potent t
108 2N]) and choline bis(trifluoromethylsulfonyl)imide ([choline][Tf2N]) showed that (1) the specific ene
109 m thick) of either plain poly(imide) or poly(imide) coated with amorphous aluminum oxide (AAO), amorp
113 d cleavage to form a Nb(V) horizontal lineNR imide complex, (i)PrN horizontal lineNb((i)PrNPPh2)3Fe-P
114 ronically similar to the previously reported imide complex, [SiP(iPr)(3)]Ru(NAr) (Ar = p-CF(3)C(6)H(4
115 led to the isolation of the formally Ru(III) imide complex, [SiP(iPr)(3)]Ru(NAr) (Ar = p-MeOC(6)H(4),
117 N-alkyl substituted bis(imino)pyridine iron imide complexes, ((iPr)PDI)FeNR ((iPr)PDI = 2,6-(2,6-(i)
123 ter norbornene imide-b-N-methyloxanorbornene imide) copolymers were prepared by pulsed-addition ring-
125 A novel concomitant enamine formation and an imide cyclization afforded the nitrogen differentially p
126 id-hydrolyzed product of helioxanthin cyclic imide derivative 9, was found to exhibit broad-spectrum
127 ction of 8 with N(3)Ar' ' afforded the amido-imide derivative Ar' 'NGaN(SiMe(3))Ar' ' (9), a gallium
128 , herein we report the synthesis of perylene imide derivatives endowed with a 1,2-diketone functional
131 me functionalities do not bind V, the cyclic imide-dioxime group of the adsorbent forms a peculiar no
133 h proteasome inhibitors and immunomodulatory imide drugs, time from diagnosis to ASCT, and cytogeneti
134 sformation between lithium amide and lithium imide during hydrogen cycling in the important Li-N-H hy
135 nic materials based on arylene imide and bis(imide) dyes, such as perylene-3,4:9,10-bis(dicarboximide
140 thylimidazolium bis(trifluoromethanesulfonyl)imide (EMMIM TFSI), is investigated in situ under applie
141 show that alane binding greatly affects the imide-enamide equilibria and that alane complexation mig
142 oieties were obtained by Evans oxazolidinone imide enolate alkylation and hydrazination/cyclization,
143 ee alkyl-substituted bis(imino)pyridine iron imides established essentially planar compounds with rel
144 ethylimidazolium bis(trifluoromethylsulfonyl)imide ([FcEMIM][TFSI]), has been investigated on both ma
146 w epimerization of the citric acid moiety or imide formation influence its function as a siderophore.
152 ning 0 to 4 methylenic units (m) between the imide group and the dendron, (3,4,5)12G1-m-PBI, is repor
154 relative to one another by attachment of the imide group of each PDI to the 4- and 5-positions of a x
156 om planarity with dihedral angles around the imide group reaching ca. -150.3 degrees (C1-N1-C2-O21 =
157 ed to the electron-withdrawing effect of the imide groups and the kinetic blocking of the most reacti
158 semifluorinated dendron was attached to the imide groups of the NBI via one, two, and three (m = 1,
163 thylimidazolium bis(trifluoromethanesulfonyl)imide has been investigated using transient cyclic volta
165 ntil now, the synthesis of N-arylated cyclic imides having six-membered rings was restricted largely
166 tonated betaine bis(trifluoromethyl sulfonyl)imide ([Hbet][Tf2N]) and choline bis(trifluoromethylsulf
167 otonated betaine bis(trifluoromethylsulfonyl)imide ([Hbet][Tf2N]) was obtained by heating and maintai
168 rocene, such as bis(trifluoromethanesulfonyl)imide, hexafluorophosphate, perchlorate, tetrafluorobora
169 yr(im)idine N functionality and preorganized imide hinge (the "CO...CO" twist) together with the inhe
170 ethylimidazolium bis(trifluoromethylsulfonyl)imide ([hmim][Tf(2)N]), was used as aqueous phase substi
171 membranes in single and multiple poly(amide-imide) hollow fibers, with H2/C3H8 and C3H6/C3H8 separat
173 lkanes with simple amides, sulfonamides, and imides (i.e., benzamides, tosylamides, carbamates, and p
174 (229 nm) ultraviolet resonance Raman (UVRR) imide II band reveals a common structural feature for ge
175 ess support a mechanism in which a transient imide (imidyl) aziridinates the diimine, which subsequen
178 hylimidazolium bis((trifluoromethyl)sulfonyl)imide in an operating EDLC with electrodes composed of p
179 ethylimidazolium bis(trifluoromethylsulfonly)imide in the poly(ether sulfone) membrane with average p
181 ns of terminal alkynes to 1,2,4-triazolium N-imides in the presence of base and Cu(I) afford pyrazolo
182 utyl imidazolium bis(trifluoromethylsulfonyl)imide, in a mixture of tetrahydrofuran and water under o
183 ersion of the compound nor the unsubstituted imide inhibit substrate cleavage, which is consistent wi
187 D magnetic measurements on the isomeric iron imides, ((iPr)PDI)FeN(1)Ad and ((iPr)PDI)FeN(2)Ad, estab
194 scalable protocols for the union of amides, imides, ketones, and oxindoles using soluble copper(II)
195 rst time that a potassium bis(fluoroslufonyl)imide (KFSI)-dimethoxyethane (DME) electrolyte forms a u
198 nt nucleophilicity of N2-derived nitride and imide ligands within a trimetallic iron system and point
200 es that contain bridged nitride and terminal imide linkages, and exhibit singlet ground-state electro
202 energy transfer are as follows: perylene-(N-imide)-linked short wire, (33 ps)(-1) and >99%; perylene
204 reactivity of the beta-diketiminato Ni(III)-imide [Me(3)NN]Ni horizontal lineNAd (1), which undergoe
208 tructural elements were identified (e.g., an imide motif or 2-octenoyl side chain), whose presence st
209 ional studies on the monomer showed that the imide N-H was a weak hydrogen bond donor, rationalizing
215 ncluding alkyl, aryl, arene, carbene, amide, imide, nitride, alkoxide, aryloxide, and oxo compounds,
217 ows the attachment of the donor group to one imide nitrogen and a solubilizing swallowtail, normally
219 connected to the PDI with the nitroxide and imide nitrogen atoms either para (1) or meta (3) to one
220 y donor (DAB) attached to either one or both imide nitrogen atoms of a perylene-3,4:9,10-bis(dicarbox
225 (PF(6)(-)) and bis[(trifluoromethyl)sulfonyl]imide (NTf(2)(-)) anions, FAP-based ILs are significantl
227 bserved when the bis(trifluoromethylsulfonyl)imide (NTf2) anion replaced the PF6(-) anion, leading to
230 from the Rh(II)-catalyzed reaction of diazo imides, on the other hand, undergo successful intramolec
231 ded Dieckmann cyclization with a concomitant imide opening, Horner-Wadsworth-Emmons olefination, and
232 rylene-monoimide dye (linked either at the N-imide or the C9 position); the transmission element cons
233 5 mm; 10-microm thick) of either plain poly(imide) or poly(imide) coated with amorphous aluminum oxi
235 l-tropane intermediate with alkoxides, metal imides, or amines was found to lead not only to the expe
237 iethyl(methyl)phosphonium bis(fluorosulfonyl)imide (P1222FSI) samples with different thermal history
238 decylphosphonium bis(trifluoromethylsulfonyl)imide ([P14,6,6,6][NTf2]) and the polymer poly(hexyl met
239 e the cis-trans isomerization of the proline imide peptide bond in many cell signaling pathways.
240 that has a 3,5-dialkoxy substitution on the imide phenyl groups (CBI-35CH), leading to "molecular po
241 ylimidazolium) bis[(trifluoromethyl)sulfonyl]imide [poly(VHIM-NTf(2))] and poly(1-vinyl-3-hexylimidaz
243 bipyridine groups covalently attached at the imide positions quantitatively yields an Fe4(PBI)6 tetra
245 mophthalimides 2 (R' = H), bearing an acidic imide proton capable of acting as a carboxylic acid bioi
246 s of the layered bulk material poly(triazine imide), PTI, followed by one-step liquid exfoliation in
247 o-OMeTAD/lithium bis(trifluoromethylsulfonyl)imide/pyridinium additives as hole transport layer were
250 erivatives with various substitutions at the imide region, and several were identified as the most pr
251 s a hexaazatriphenylene "platform" and three imide residues on its concave side carrying flexible alk
257 nzobacteriochlorins containing N-substituted-imide ring system produced enhanced photosensitizing eff
261 solvents and the lithium bis(fluorosulfonyl)imide salt enables the high-rate cycling of a lithium me
265 neglycol ether chain, and aryl group) at the imide sites as well as at the bay regions are described
266 from 4H-pyrido[1,3]oxazin-4-one precursors (imide sodium salts) was developed and led to the desired
267 of a bimolecular coupling mechanism of metal imide species, as shown in the related [SiP(iPr)(3)]Fe s
269 the sugar, rather than the modifications in imide structure on the indolocarbazole ring, is a key el
271 le host wider than the corresponding urea or imide structures, and longer alkanes can be accommodated
272 est as it provides access to unsymmetrically imide-substituted 1,7-dibromoperylene derivatives, which
273 atom transfer reactions of an oxazolidinone imide substrate, 1, derived from alpha-bromo acetic acid
275 cessfully translated to the bacteriopurpurin imide system 19 (lambdamax: 792 nm) and within both seri
276 and DNA binding properties of a bis-naphthyl imide tetracationic diviologen compound NI(CH2)3V(2+)(CH
277 dazolium (C2mim) bis(trifluoromethylsulfonyl)imide (Tf2N) and its mixtures with carbon dioxide in ord
278 s en-abled by a bis(trifluoromethanesulfonyl)imide (TFSI-) anion-based room temperature ionic liquid
279 er electrolyte, bis(trifluoromethanesulfonyl)imide (TFSI-), yielded transistors that showed clear cur
280 th Tyr-1771 of Na(V)1.2 and a polar amide or imide that interacts with the aromatic ring of Phe-1764
281 on to accessing a wide variety of alpha-keto-imides, the RuO2-NaIO4 protocol provides a novel entry t
282 col involving ethanethiolate exchange of the imide to the corresponding thioester, followed by a stan
285 lytetrafluoroethylene (Teflon) and polyamide-imide (Torlon), discharge when the like-charged beads ar
290 ic addition of PhSCF(2)SiMe(3) (1) to chiral imides was achieved in satisfactory yields to provide mi
291 However, a series of N-farnesyl lactams and imides was converted to the desired phosphonates through
292 imethylammonium bis(trifluoromethanesulfonyl)imide, was synthesized and characterized by (1)H NMR, (1
294 -bonding receptors along the poly(norbornene imide) were synthesized either also via ROMP by terminat
296 arboxylate leads to an intermediate carbonyl imide, which can react with a variety of amines to affor
297 intermediates in the reactions of amides and imides with haloarenes catalyzed by copper complexes con
300 ocol allows direct C2 arylation of azolium N-imides without the use of specialized reagents together
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