IN DEFENSE OF POLYVALENCE IN 1 COR 12,13C: EΠOTIΣΘHMEN

被引：0
|
作者：
Cook, John Granger [1 ]
机构：
[1] LaGrange Coll, 601 Broad St, La Grange, GA 30240 USA
来源：
BIBLICA | 2022年 / 103卷 / 03期
关键词：
D O I：
10.2143/BIB.103.3.3291157
中图分类号：
B9 [宗教];
学科分类号：
010107 ;
摘要：
1 Cor 12,13c has generated an intriguing exegetical debate that remains ongoing. Scholars have been unable to demonstrate conclusively whether eποτίσθημεν means “we were saturated” or “we were made to drink”. In addition, interpreters have been unable to conclusively show whether the reference of 12,13c is to baptism or the Eucharist. These ambiguities are not ultimately fatal, however. John Chrysostom used all four of these possible readings of the phrase in his homily on 1 Cor 12,13. It is likely that Paul himself was intentionally responsible for the polyvalence of the text. © 2022 Peeters Publishers. All rights reserved.
引用
收藏
页码：404 / 426
页数：23
相关论文
共 50 条
  • [21] Measurement of site-specific 13C/12C stable isotope ratios from 13C satellite peaks in 1H NMR spectra
    Cort, John
    Cho, Herman
    Kempler, Paul
    Metaxas, Athena
    Schultz, J.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2015, 250
  • [22] Studies on the synthesis of bitungolides A-E: Synthesis of the C(1)-C(12) fragment
    Xu, Yanfen
    Huo, Xing
    Li, Xinyun
    Zheng, Huaiji
    She, Xuegong
    Pan, Xinfu
    SYNLETT, 2008, (11) : 1665 - 1668
  • [23] REACTION 13C(3HE, A)12C IN ENERGY RANGE E3HE = 1,8 TO 5,4 MEV
    BOEHLE, K
    MEYER, V
    MULLER, HH
    HELVETICA PHYSICA ACTA, 1971, 44 (03): : 367 - &
  • [24] Identification of Turkish extra virgin olive oils produced in different regions by using NMR (1H and 13C) and IRMS (13C/12C)
    Sevim, Didar
    Koseoglu, Oya
    Ertas, Hasan
    Ozdemir, Durmus
    Ulas, Mehmet
    Gunnaz, Salih
    Celenk, Veysel Umut
    JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 2023, 100 (05) : 355 - 367
  • [25] 1H and 13C NMR spectral analysis of (E)-asarone and its isomers
    Siergiejczyk, L
    Poplawski, J
    Lozowicka, B
    Dubis, A
    Lachowska, B
    MAGNETIC RESONANCE IN CHEMISTRY, 2000, 38 (12) : 1037 - 1038
  • [26] The 13C/12C and 2H/1H ratios of trichloroethene, tetrachloroethene and their metabolites
    Ertl, S
    Seibel, F
    Eichinger, L
    Frimmel, FH
    Kettrup, A
    ISOTOPES IN ENVIRONMENTAL AND HEALTH STUDIES, 1998, 34 (03) : 245 - 253
  • [27] EXPERIMENTAL AND THEORETICAL INVESTIGATION OF E1-ELECTROEXCITATION OF 3.08 MEV LEVEL IN 13C
    TOMASELLI, M
    GRUNBAUM, L
    BEER, GA
    CLERC, HG
    WITTWER, G
    PHYSICS LETTERS B, 1969, B 29 (09) : 579 - +
  • [28] 1,2-, 1,7-and 1,12-Dicarba-closo-dodecaborane(12) Derivatives Revisited by 13C NMR Spectroscopy and DFT Calculations. First Observation of Isotope-Induced Chemical Shifts 1Δ10/11B(13C), and the Signs and Magnitudes of Coupling Constants 1J(13C,13C) and 1J(13C,11B)
    Wrackmeyer, Bernd
    Hernandez, Zureima Garcia
    Lang, Julian
    Tok, Oleg L.
    ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 2009, 635 (08): : 1087 - 1093
  • [29] Novel 16-membered macrolides modified at C-12 and C-13 positions of midecamycin A1 and miokamycin.: Part 1:: Synthesis and evaluation of 12,13-carbamate and 12-arylalkylamino-13-hydroxy analogues
    Miura, Tomoaki
    Kurihara, Ken-ichi
    Furuuchi, Takeshi
    Yoshida, Takuji
    Ajito, Keiichi
    BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (07) : 3985 - 4002
  • [30] Neutron ambient dose equivalent from 5 MeV/u 10,11B, 12,13C and 16,18O projectiles incident on a thick Al target
    Sunil, C.
    Shanbhag, A. A.
    Nandy, M.
    Tripathy, S. P.
    Sahoo, G. S.
    Joshi, D. S.
    Kale, R. M.
    Sarkar, P. K.
    Sharma, D. N.
    RADIATION MEASUREMENTS, 2012, 47 (10) : 1035 - 1043
12345